Patent Application
20100041658
The invention relates to hydroxyphenyl derivatives and a process for making the same. It also relates to the biological applications thereof, particularly as anti-bacterial and/or anti-parasites agents.
The invention more particularly relates to Triclosan derivatives. Triclosan (TCL) 5-chloro-2-(2,4-dichloro-phenoxy)-phenol (A) is a broad-spectrum biocide that has been in use for over 30 years, mainly as a component of antimicrobial wash products in health-care settings, of formula (A)
More recently, Triclosan has found extensive use in consumer products such as toothpaste, mouthwashes, deodorants, hand soaps, and lotions. It is also incorporated in children's toys, cutting boards, and the plastic film used to wrap meat products. Until recently, it was thought that Triclosan, being a small hydrophobic molecule, was absorbed via diffusion into the bacterial cell wall and that unspecific disruption of the cell wall was the mechanism by which Triclosan exhibited its antibacterial activity. However, the first evidence that Triclosan inhibits fatty acid biosynthesis came when a strain of E. coli resistant to Triclosan was isolated, and the resistance was mapped to the fabI gene which codes for the E. coli trans enoyl-acyl carrier protein reductase (ENR). Fatty acid biosynthesis in bacteria is essential to the production of a number of lipid-containing components including the cell membrane. The bacterial fatty acid synthase system (FASII) utilizes discrete monofunctional enzymes that operate in conjunction with acyl carrier protein (ACP)-associated substrates. Mammalian fatty acid synthase (FASI) differs from FASII in that lipid biosynthesis is mediated by a single multifunctional enzyme-ACP complex. The differences in prokaryote and eukaryote fatty acid biosynthesis offer an attractive opportunity for selective FASII inhibition. FabI is an enoyl-ACP reductase that catalyzes the ultimate and rate-limiting step of the chain elongation process of FASII. The reaction involves the conjugate reduction of an enoyl-ACP to the corresponding acyl-ACP using the cofactor NAD(P)H as a hydride source.
Subsequently, extensive biochemical and structural studies have been performed to substantiate Triclosan as a specific E. coli FabI inhibitor. Two ENR isoforms, FabK and FabL, have been discovered in the gram-positive bacteria, Streptococcus pneumoniae and Bacillus subtilis, respectively. FabK is resistant to Triclosan, whereas FabL is reversibly inhibited by Triclosan. Triclosan also directly inhibits the FabI from Staphylococcus aureus, Haemophilus influenzae, the ENR from Mycobacterium tuberculosis, InhA, and the ENR from Plasmodium falciparum, the malarial parasite.
Since the discovery of FabI as the bacterial target of Triclosan, several specific inhibitors not structurally related to TCL have been reported, few of them displaying antibacterial activities.
Some analogues of Triclosan itself have been described in separate chemo-enzymatic studies of the Triclosan mode of action against FabI. Especially, the antibacterial activity of several 2-hydroxydiphenyl ethers hexachlorophene and 2-hydroxydiphenylmethanes as well as 5-alkylated, -fluorinated or -formylated derivatives have been determined. On the other hand, before the discovery of the potent inhibition of FabI by TCL, some modifications of the dichlorophenol part of TCL were also reported. For instance broad spectrum, but non specific antibacterial and antifungal derivatives were reported by introducing a pyridine instead of a phenyl ring.
In contrast to TCL, which displays a broad spectrum biocidal effect with no distinction between microorganisms, new TCL derivatives that would target only the microorganisms which carry the FabI enzyme such as S. aureus or E. coli would be selective antibacterial or antiparasitic agents of interest with no antibacterial effect or selective pressure against other bacterial species.
The inventors have found that specific substitutions of hydroxyphenyl derivatives having triclosan basic structure lead to derivatives that surprisingly display a selective and narrow spectrum of activity against relevant pathogens, particularly bacteria or parasites.
An object of the invention is then to provide new substituted hydroxyphenyl derivatives which selectively inhibit the growth of bacteria carrying Fab enzymes such as FabI, FabL, FabK, InhA.
Another object of the invention is to provide a process for the synthesis of said derivatives.
Still another object is to take advantage of the biological properties of said molecules to provide means, i.e. pharmaceutical compositions and methods, particularly useful for treating microbial infections.
The hydroxyphenyl derivatives of the invention have formula (A)
wherein
if T1 and T5 are independently N or C—R, R being H, methyl, ethyl, halo, then
When R1 is an heterocycle and more specifically a pyridine, the invention also includes the N-oxide form.
“Alkyl” as applied herein means an optionally substituted alkyl group and preferably methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl and t-butyl, pentyl, n-pentyl, isopentyl, neopentyl,hexyl and octyl.
“Alkoxy” and “thioalkyl” mean any O or S atom substituted by a substituted or not alkyl group.
“Aryloxy”, “thioaryl”, “NH-aryl” mean any O, S, N substituted by a substituted or not aryl, or heterocyclic group.
“Aryl” (or “Ar”) means phenyl or naphtyl optionally substituted by R.
“Alkenyl” and “alkynyl” mean optionally substituted C═C or C≡C groups.
“Halogen” or “halo” means F, Cl, Br, and I.
“Aliphatic heterocycle” or “heterocycle” indicates an optionally substituted five or six membered monocyclic ring, or a nine or ten-membered bicyclic ring containing one to three heteroatoms chosen from the group of nitrogen, oxygen and sulfur, which are stable and available by conventional chemical synthesis. Illustrative heterocycles are for example selected in the group comprising benzofuryl, benzimidazolyl, benzopyranyl, benzothienyl, furyl, imidazolyl, indolinyl, morpholinyl, piperidinyl, piperazinyl, pyrrolyl, pyrrolidinyl, tetrahydropyridinyl, pyridinyl, thiazolyl, thienyl, quinolinyl, isoquinolinyl, and tetra- and perhydro-quinolinyl and isoquinolinyl, pyrazinyl, pyrazidinyl, triazinyl, purine, indolyl, indazolyl, pyrimidinyl, pyridonyl, oxazolyl, tetrahydropyranyl, tetrahydrofuranyl.
The invention more particularly relates to hydroxyphenyl derivatives having formula (I)
wherein
Z4, Z5, Z6, Z7 and Z8 independently are C or N with a maximum of three N, R1 being possibly substituted by 1 to 3 R identical or different, R being selected from the group comprising H, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, 5 or 6 membered monocyclic heteroaryl or aliphatic heterocycle containing 1 to 3 heteroatoms selected from N, O and S, COORa, CORa, CONRaRb, OCORa, CN, ORa, NRaRb, CRa═NORb, NRaCORb, NRaCOORb, OCONRaRb, NRaCONRbRc, SRa, SO2Ra, SO2NRaRb, NRaSO2Rb and NRaC(S)NRbRc, all being possibly substituted by R′, or R is C1-C4 fluoro-alkyl, or R is fluor when R1 is phenyl, or R is halogeno when R1 is nitrogenous heteroaryl,
According to a first family, the invention particularly relates to derivatives of formula (I) wherein R1 is a 6-membered monocyclic heteroaryl group such as above defined. Preferably, the nitrogeneous heteroaryl with one or 3 nitrogen atoms is selected in the group comprising a pyridine, a pyrimidine, a pyridazine, a pyrazine or a triazine.
In particularly preferred derivatives of said first family, R1 is a substituted heteroaryl group such as above defined.
Advantageously, the nitrogeneous heteroaryl group is substituted by one or several substituents selected in the group comprising F, CORa, ORa, NRaRb, alkynyl, SO2Ra, NRaSO2Rb, SO2NRaRb, NRaCOORb and CRa═NORb.
According to a second family, the invention particularly relates to derivatives of formula (I) wherein R1 is a phenyl group.
Particularly preferred derivatives of said second family are substituted by one or several substituents selected in the group comprising F, CORa, ORa, NRaRb, alkynyl, SO2Ra, NRaSO2Rb, SO2NRaRb, NRaCOORb and CRa═NORb.
In a preferred embodiment, in the above defined derivatives of said first and/or second family, Z2 is fluor. The fluorine atom being advantageously positioned in para of the OH group of compound of formula I when Y═H to prevent the in vitro or in vivo oxidation of the phenolic compound into the corresponding quinone.
According to another embodiment, Z6 is a carbon atom substituted by R as defined above, R being different from H, alkyl, halogen, NH2, OH, CONH2, or fluoro alkyl and all the other definitions are as defined with respect to formula (I).
According to still another preferred embodiment, Z4 or Z5, or Z7 or Z8, are carbon atoms substituted by NRaRb or ORa, ORa being different from OH and all the other definitions are as defined with respect to formula (I).
In a further embodiment, Z5 or Z7 is a carbon atom substituted by R, R being different from H and all the other definitions are as defined with respect to formula (I).
According to an other embodiment family, the invention particularly relates to derivatives of formula (I) wherein, R2 is a C1-C8alkyl-heteroaryl or a C1-C8alkyl-ORa, ORa being different from OH.
In a more preferred embodiment, Y represents H.
Also included in this invention are compounds in which Y is different from H, Y being a labile chemical group able to regenerate in vivo the free phenol compounds of formula I with Y being H such C(O)Ra, C(O)ORa, C(O)NRa, C(O)NRa,Rb, P(O)(OH)2, COCHRaNRbRc
It will be understood that the above defined embodiment can be used in combination with any one of the other defined embodiments.
The invention also relates to a process for making the above defined derivatives.
In a first embodiment of the invention, said process comprises the steps of
wherein R1, R2 and Z1, Z2, Z3 are as above defined, R3 represents an alkyl group, and A is a reactive group such as an halogen or a nitro capable of reacting with the OH group of (II) under basic conditions known to the one skilled in the art to give a derivative of formula (III)
Alternatively, the derivatives of formula (I) are advantageously obtained from the protected phenols of formula (II) by introducing a R4 group different from R3=alkyl which can be smoothly remove in a non restrictive manner by hydrogenation, acidic conditions or treatment with fluoride derivatives to generate compound of formula (I) according to a process comprising:
and
According to a second embodiment, compounds of formula (I) with Z2=F can be obtained according to the following synthetic scheme 1 by a process comprising:
or alternatively,
According to a third embodiment, the invention also comprises a process wherein a compound of formula (XIII), corresponding to compounds of formula (III), (VI), (VII), (X) or (I) in which R2 is vinyl and R5 is R3 or R4 as above defined or H, is reduced by hydrogenation with palladium on charcoal (according to scheme 4) to give the R2=ethyl compound derivative (XIV), corresponding to compounds of formula (III), (VI), (VII), (X) or (I) which can be further deprotected according to the above process when R5=R3 or R4.
According to a fourth embodiment, the process of the invention for making a compound of formula (I) consists of converting, derivatives of formula I in which Y═H advantageously by methods known by one skilled of the art into a compound in which Y is C(O)Ra, CO(O)Ra, C(O)NRa,Rb, P(O)(OH)2, and COCHRaNRbRc.
As illustrated by the examples given hereinafter, the above disclosed phenol derivatives of the invention have valuable biological properties.
They are particularly useful as antibacterial agents having a selective spectrum of activity in vitro against standard bacterial strains which are used to screen for activity against pathogenic bacteria. Notably, the derivatives of the present invention show a high activity against bacteria carrying Fab enzymes such as FabI, FabL, FabK, InhA. Particularly against Staphyloccus aureus including multiresistant strains, Escherichia coli, Helicobacter pylori and also bacteria such as Mycobacterium tuberculosis carrying homologous Fab enzymes such as InhA or other organisms such as Plasmodium falciparum. Said derivatives are then particularly suitable as active principle of drugs.
The invention thus also relates to compositions comprising a phenol derivative of formula (I) such as above defined for use as drug.
It also relates to pharmaceutical compositions comprising a phenol derivative of formula (I) such as above defined in combination with a pharmaceutically acceptable carrier.
Said pharmaceutical compositions are formulated to be administered under oral, injectable, parental routes, with doses appropriate for the patient to be treated.
The compositions of the invention may conveniently be presented in unit dosage form and may be prepared by any methods well known in the art of pharmacy. The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will generally be that amount of the compound which produces a therapeutic effect.
A suitable daily dose of the compounds of the invention will be that amount of the compound that is the lowest dose effective to produce a therapeutic effect. Generally, topical, intravenous and subcutaneous doses of the compositions of this invention for a patient, when used for the indicated effects, will range from about 0.0001 to about 100 mg per kilogram of body weight per day, given in one or several doses administered separately at appropriate intervals throughout the day, optionally, in unit dosage forms.
Said compositions are particularly useful to treat human or animal infections by microbial pathogens such as E. coli, H. pylori or S. aureus or M. tuberculosis and parasites such as Plasmodium falciparum.
Said compositions are also useful in multitherapy, in combination with other drugs, for example with antibiotics.
The invention also relates to a method of treatment of microbial infections which comprises administering to a patient in need thereof an efficient amount of a pharmaceutical composition such as above defined.
Other characteristics and advantages of the invention are given in the examples hereafter wherein it is referred to
Synthesis of example compounds:
Proton nuclear magnetic resonance (1H NMR) spectra were recorded at either 300 or 400 MHz, and chemical shifts are reported in parts per million (δ) downfield from the internal standard tetramethylsilane (TMS). Abbreviations for NMR data are as follows: s=singlet, d=doublet, t=triplet, q=quadruplet, qt=quintuplet, se=sextuplet, m=multiplet, dd=doublet of doublets, dt=doublet of triplets, br=broad. J indicates the NMR coupling constant measured in Hertz. CDCl3 is deuteriochloroform, DMSO-d6 is hexadeuteriodimethylsulfoxide, and CD3OD is tetradeuteriomethanol. Mass spectra were obtained using either electrospray (ESI) or atmospheric pressure photoionization (APPI) techniques. Analtech Silica Gel GF and E. Merck Silica Gel 60 F-254 thin layer plates were used for thin layer chromatography. Flash chromatography was carried out on Flashsmartpack cartridge, irregular silica 40-60 μm or spherical silica 20-40 μm
TLC refers to thin layer chromatography, MS refers to mass spectra, HPLC refers to high pressure liquid chromatography, NMR refers to nuclear magnetic resonance, APT refers to attached proton test, HSQC refers to heteronuclear single quantum correlation, NOESY refers to nuclear Overhauser enhancement spectroscopy.
Certain reagents and radical groups are abbreviated herein are abbreviated herein. t-Bu refers to the tertiary butyl radical, Boc refers to the t-butyloxycarbonyl radical, Ph refers to the phenyl radical, Cbz refers to the benzyloxycarbonyl radical, Bn refers to the benzyl radical, Me refers to methyl, Et refers to ethyl, Ac refers to acetyl, Nph refers to 1- or 2-naphthyl and cHex refers to cyclohexyl. DCC refers to dicyclohexylcarbodiimide, DMAP refers to 4-dimethylaminopyridine, EDC refers to 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride, HOBt refers to 1-hydroxybenzotriazole, THF refers to tetrahydrofuran, DIEA refers to diisopropylethylamine, DEAD refers to diethyl azodicarboxylate, PPh3 refers to triphenylphosphine, DIAD refers to diisopropyl azodicarboxylate, DME refers to dimethoxyethane, DMF refers to dimethylformamide, NBS refers to N-bromosuccinimide, Pd/C refers to a palladium on carbon catalyst, PPA refers to polyphosphoric acid, DPPA refers to diphenylphosphoryl azide, BOP refers to benzotriazol-1-yloxy-tris(dimethyl-amino)phosphonium hexafluorophosphate, TEA refers to triethylamine, TFA refers to trifluoroacetic acid, PCC refers to pyridinium chlorochromate, TBAF refers to tetrabutyl ammonium fluoride, Tos refers to Tosyl and TosCl refers to tosyl Chloride, BOM refers to p-methoxybenzyl, MOM refers to methoxy-methyl, MEM refers to methoxy-ethoxymethyl, SEM refers to trimethyl-silyl-ethoxymethyl, THP refers to tetrahydropyranyl, TSI refers to triethylsilyl, TBDMS refers to tButyl-dimethyl-silyl, DCM refers to dichloromethane, CAN refers to acetonitrile, Pet ether refers to petroleum ether.
To a suspension of K2CO3 (2.4 mmol; 331 mg) in anhydrous DMF (1 mL) under argon, was added 2-methoxy-4-propylphenol (1 mmol; 0.16ml) followed by 2.6-Dichloro-3-nitropyridine (1 mmol; 176 mg). The reaction mixture was stirred at 40° C. over 48 H.
After quenching with NaOH (0.1N; 3 mL), the mixture was extracted with ethyl acetate (3*3 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give a yellow solid (480 mg; 1.49 mmol; 74%), used without further purification. 240 mg of that solid (0.75 mmol) were dissolved in THF (3 mL) under argon. Palladium on activated carbon (50 mg) was added then the reaction was flushed twice with hydrogen, then left to stir overnight. The reaction mixture was then filtered on celite, and then rinsed with ethyl acetate (3*5 mL), to give a mixture of regioisomers. After purification by preparative TLC (dichloromethane), the regioisomers were isolated as light yellow oils. (A: 40 mg, 0.14 mmol, B: 30 mg, 0.1 mmol, global yield: 32%)
A: 1H NMR (CDCl3) δ (ppm): 7.08 (d, 1H, J=8.3 Hz); 6.97 (d, 1H, J=7.9 Hz); 6.76 (m, 2H);
6.59 (d, 1H, J=8.5 Hz); 2.59 (t, 2H, J=7.6 Hz,); 1.65 (se, 2H, J=7.4 Hz); 0.98 (t, 3H, J=7.2 Hz).
B: 1H NMR (CDCl3) δ (ppm): 7.6 (d, 1H, J=7.9 Hz); 6.98 (d, 1H, J=7.9 Hz); 6.79 (m, 3H);
2.59 (t, 2H, J=7.6 Hz,); 1.67 (se, 2H, J=7.4 Hz); 0.97 (t, 3H, J=7.2 Hz).
To a solution of 6-chloro-2-(2-methoxy-4-propyl phenoxy)pyridin-3-amine (0.1 mmol; 30 mg) under argon, in dichloromethane (2 mL), cooled to −78° C., was added BBr3 (0.5 mmol; 0.5 mL) dropwise. The reaction mixture was allowed to stir for 5 hr, with gradual warming to −20° C. At −20° C., the reaction was hydrolysed with saturated NH4Cl (4 mL), extracted with dichoromethane (3*10 mL). Combined organic phases dried over Na2SO4, concentrated in vacuo, to give the desired product as a light brown solid without further purification (27 mg 0.1 mmol; 97%).
1H NMR (CDCl3) δ (ppm): 7.06 (d, 1H, J=8.0 Hz); 6.99 (d, 1H, J=8.2 Hz); 6.89(m, 2H); 6.69 (d, 1H, J=8.1 Hz); 2.52 (t, 2H, J=7.7 Hz,); 1.64 (se, 2H, J=7.5 Hz); 0.93 (t, 3H, J=7.4 Hz).
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-chloro-6-(2-methoxy-4-propylphenoxy)pyridin-3-amine (0.14 mmol; 40 mg) the title compound (30 mg; 0.11 mmol; 77%). was prepared without any purification as a light brown solid.
1H NMR (CDCl3) δ (ppm): 7.13 (d, 1H, J=8.4 Hz), 6.94 (d, 1H, J=8.2 Hz); 6.88(s, 1H); 6.74 (d, 1H, J=8.4 Hz); 6.66 (d, 1H, J=8.2 Hz); 2.52 (t, 2H, J=7.6 Hz,), 1.63 (se, 2H, J=7.5 Hz); 0.95 (t, 3H, J=7.3 Hz).
To a suspension of NaH (1.2 mmol; 50 mg) in anhydrous DMSO (1 mL) under argon, was added 4-ethyl-2-methoxyphenol (1 mmol; 152.2 mg) followed by 2,6-difluoropyridine (1 mmol; 0.1 ml). The reaction mixture was stirred at 120° C. overnight. After quenching with NaOH (0.1N; 3 mL), the mixture was extracted with dichloromethane (3*5 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give the title compound as a light yellow oil (250 mg; 1 mmol; 100%), used without further purification.
MS(ES): m/e 248 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-(4-ethyl-2-methoxyphenoxy)-6-fluoropyridine (250 mg, 1 mmol) the title compound (80 mg, 34%) was prepared as a white solid after purification by flash chromatography on silica gel (gradient dichloromethane/methanol).
MS(ES): m/e 234 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.77 (q, 1H, J1=7.9 Hz, J2=8.0 Hz); 7.01 (d, 1H, J=8.2 Hz,); 6.92 (d, 1H, J=1.9 Hz); 6.75 (td, 2H, J1=8.2 Hz, J2=2.0 Hz); 6.64 (dd, 1H, J1=7.9 Hz, J2=2.4 Hz); 2.62 (q, 2H, J1=7.6 Hz, J2=7.6 Hz); 1.23 (t, 3H, J=7.6 Hz).
Alternatively compound of example 3 can be synthesized starting from 2-Benzyloxy-4-ethyl-phenol instead of 4-ethyl-2-methoxyphenol according to the following procedure:
a′) To a solution of 2-methoxy-4-ethylphenol (26.3 mmol; 4.0 g), NaI (5.25 mmol; 788 mg), and K2CO3 (28.9 mmol; 3.98 g), under argon, in acetonitrile (20 mL) was added tosyl chloride (27.6 mmol; 5.24 g). The reaction mixture was stirred at 70° C. for 30 hr, then quenched with NaOH (0.1N; 50 mL), and extracted with ethyl acetate (3*20 mL). Combined organic phases were washed with saturated NaHCO3 sat. (50 mL) then water (50 mL), dried over MgSO4 and concentrated in vacuo. The crude was recristallized in cyclohexane (10 mL) to yield a brown oil (5.53 g; 18.1 mmol; 68%) engaged without further purification in step b′.
b′) To a solution of 5 g of Toluene-4-sulfonic acid 4-ethyl-2-methoxy-phenyl ester (16.3 mmol), under argon, in dichloromethane (15 mL), cooled to −78° C., was added BBr3 (35 mmol; 35 mL) dropwise. The reaction mixture was allowed to stir for 6 hr, with gradual warming to −20° C. At −78° C., the reaction was hydrolysed with saturated NH4Cl (30 mL), extracted with dichoromethane (2*10 mL). Combined organic phases were washed with 100 mL of satured NaHCO3, dried over Na2SO4, concentrated in vacuo, the title compound (1.97 g; 41%) was obtained as a colourless oil, after purification on silica gel (dichloromethane/cyclohexane: gradient).
1H NMR (CDCl3) δ (ppm): 7.76 (d, 2H, J=8.1 Hz); 7.34 (d, 2H, J=7.9 Hz); 6.84 (s, 1H); 6.65 (d, 1H, J=8.4 Hz); 6.58 (d, 1H, J=6.8 Hz); 5.86 (sl, 1H); 2.56 (q, 2H, J=7.6 Hz); 2.46 (s, 3H); 1.18 (t, 3H, J=7.6 Hz).
To a solution of 4-ethyl-2-hydroxyphenyl-4-methylbenzenesulfonate (5 mmol; 1.46 g) under argon, in acetone (10 mL), were added K2CO3 (6 mmol; 0.83 g), NaI (1 mmol; 0.15 g), and benzylbromide (5.5 mmol; 0.65 mL). The reaction was stirred at 40° C. for 5 hr. The reaction mixture was concentrated then hydrolysed with NH4Cl sat. (10 mL) and extracted with ethyl acetate (3*5 mL). Combined organic phases were washed with saturated NaHCO3 (10 mL), dried over Na2SO4, concentrated. The residue was purified on silica gel (dichloromethane/cyclohexane: gradient) to yield the title compound as a clear oil (1.68 g; 4.39 mmol; 87%).
1H NMR (CDCl3) δ (ppm): 7.69 (d, 2H, J=8.3 Hz); 7.34 (m, 5H); 7.11 (m, 3H); 6.74 (m, 2H); 4.87 (s, 2H); 2.59 (q, 2H, J=7.6 Hz); 2.37 (s, 3H); 1.19 (t, 3H, J=7.6 Hz).
To a solution of 2-(benzyloxy)-4-ethylphenyl-4-methylbenzenesulfonate methylbenzenesulfonate (0.26 mmol; 100 mg) under argon, in methanol (2 mL), was added magnesium (2.61 mmol; 0.63 g). The reaction was stirred at room temperature overnight. The reaction mixture was hydrolysed with HCl 1N (3 mL) and extracted with ethyl acetate (3*5 mL). Combined organic phases were washed with saturated NaHCO3 (10 mL), dried over Na2SO4, concentrated. The residue was purified with preparative TLC (dichloromethane/cyclohexane: 9/1) to yield the title compound as a yellow oil (48 mg; 0.21 mmol; 80%).
MS (ES) m/e 229 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.43 (m, 5H); 6.90 (d, 1H, J=8.0 Hz); 6.82 (s, 1H); 6.75 (d, 1H, J=8.0 Hz); 5.55 (s, 1H); 5.12 (s, 2H); 2.61 (q, 2H, J=7.6 Hz); 1.25 (t, 3H, J=7.6 Hz).
To a suspension of K2CO3 (0.25 mmol; 35 mg) in anhydrous acetonitrile (2 mL) under argon, was added 2-Benzyloxy-4-ethyl-phenol (48 mg; 0.21 mmol) followed by 2,6-difluoropyridine (100 μL; 1.10 mmol). The reaction mixture was stirred at 80° C. overnight.
Concentrated under argon, washed with NH4Cl (0.1N; 3 mL), the mixture was extracted with ethyl acetate (3*3 mL). Combined organic phases were washed with NaHCO3 dried over MgSO4, concentrated in vacuo, to give the title product as a light oil (28.5 mg; 42%), after purification by preparative TLC (cyclohexane/ethyl acetate: 9/1).
1H NMR (CDCl3) δ (ppm): 7.70 (q, 1H, J=8.0 Hz); 7.27 (m, 3H); 7.17 (d, 2H, J=5.8 Hz); 7.11 (d, 1H, J=8.0 Hz); 6.90 (s, 1H); 6.86 (d, 1H, J=8.1 Hz); 6.73 (d, 1H, J=7.5 Hz); 6.56 (dd, 1H, J1=7.8 Hz, J2=2.4 Hz); 5.06 (s, 2H); 2.66 (q, 2H, J=7.6 Hz); 1.27 (t, 3H, J=7.6 Hz).
2-[2-(benzyloxy)-4-ethylphenoxy]-6-fluoropyridine (28 mg; 0.09 mmol) was dissolved in ethanol (4 mL), under argon. Palladium on charcoal (4 mg; 0.02 mmol) was added and the reaction was flushed twice with hydrogen, then left to stir overnight at room temperature. The reaction mixture was filtered on celite, then rinsed with methanol (3*3 mL). Concentration yielded a white solid (25 mg; 98%) of title compound.
MS (ES) m/e 234 (M+H)+.
To a suspension of KOH (2 mmol; 112 mg) in anhydrous DMF (1 mL) under argon, was added 4-(2-hydroxyethyl)-2-methoxyphenol (1 mmol; 168 mg) followed by 2,6-Difluoropyridine (1 mmol; 0.1 ml). The reaction mixture was stirred at 110° C. for 20 h.
After quenching with NaOH (0.1N; 3 mL), the mixture was extracted with ethyl acetate (3*5 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give a clear oil (50 mg; 0.14 mmol; 28%), after purification by flash chromatography on silica gel (gradient cylohexane/dichloromethane).
MS(ES): m/e 359 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-fluoro-6-(4-{2-[(6-fluoropyridin-2-yl)oxy]ethyl}-2-methoxyphenoxy)pyridine (50 mg, 0.14 mmol) the title compound (20 mg, 30%) was prepared as a white solid after purification by preparative TLC (dichloromethane/methanol—9/1).
MS(ES): m/e 234 (M+H)+.
1H NMR (CDCl3) δ (ppm): 7.76 (q, 1H, J1=7.9 Hz, J2=8.0 Hz); 7.62 (q, 1H, J1=8.3 Hz, J2=7.99); 7.02 (m, 2H); 6.83 (dd, 1H, J1=8.2 Hz, J2=2.0 Hz); 6.76 (d, 1H, J1=7.8 Hz,); 6.65 (dd, 1H, J1=7.7 Hz, J2=1.8 Hz); 6.59 (dd, 1H, J1=8.0 Hz, J2=1.1 Hz); 6.45 (dd, 1H, J1=7.7 Hz, J2=2.1 Hz); 6.09 (s, 1H); 4.47 (t, 2H, J=6.9 Hz); 3.03 (t, 2H, J=6.9 Hz).
According to the procedure of example 4(a) except substituting 4-(2-hydroxyethyl)-2-methoxyphenol for 2-methoxy-4-propylphenol (2.1 mmol; 0.34 mL) the title compound (449 mg; 86%) was prepared as a white solid, after purification by silica gel chromatography (gradient cyclohexane/dichloromethane).
MS (ES) m/e 262 (M+H)+
To a solution of 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine (1.7 mmol; 449 mg) under argon, in dichloromethane (1.5 mL), cooled to −78° C., was added BBr3 (17 mmol; 1M in CH2Cl2; 17 mL). The reaction mixture was allowed to stir overnight, with gradual heating to room temperature. At −20° C., the reaction was hydrolysed with saturated NH4Cl (3 mL), extracted with ethyl acetate (3*10 mL). Combined organic phases were dried over MgSO4, concentrated in vacuo. The residue was chromatographed on silica gel (gradient cyclohexane/dichloromethane) to give the desired product as a white solid (160 mg; 0.65 mmol; 38%).
MS (ES) m/e 248 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.78 (q, 1H, J=8 Hz); 7.02 (d, 1H, J=8.4 Hz); 6.92 (d, 1H, J=2 Hz); 6.76 (ta, 2H, J=9.2 Hz); 6.65 (dd, 1H, J1=8 Hz, J2=2.4 Hz); 2.58 (t, 2H, J=7.6 Hz); 1.67 (s, 2H, J=7.6 Hz); 0.98 (t, 3H, J=7.2 Hz).
Aletrnatively compound of example 5 can be synthesized starting from the 2-(benzyloxy)-4-propylphenol instead of -methoxy-4-propylphenol using the same protocol as example 3 step f) and g).
To a solution of 2-methoxy-4-propylphenol (10.0 mmol; 1.6 mL), NaI (1.0 mmol; 150 mg), and K2CO3 (11.0 mmol; 1.52 g), under argon, in acetonitrile (20 mL) was added tosyl chloride (10.5 mmol; 2.0 g). The reaction mixture was stirred at 70° C. for 36 hr, then quenched with NaOH (0.1N; 3 mL), and extracted with ethyl acetate (2*10 mL). Combined organic phases were washed with saturated NaHCO3 sat. (5 mL), dried over MgSO4, concentrated in vacuo. The crude was chromatographed on silica gel (gradient cyclohexane/dichloromethane) to yield the desired compound as a clear oil (2.13 g; 6.6 mmol; 66%).
MS (ES) m/e 321 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.77 (d, 2H, J=8.2 Hz); 7.31 (d, 2H, J=8.0 Hz); 7.03 (d, 1H, J=8.2 Hz); 6.70 (m, 2H); 3.57 (s, 3H); 2.54 (t, 2H, J=7.7 Hz); 2.46 (s, 3H); 1.63 (se, 2H, J=7.6 Hz); 0.95 (t, 3H, J=7.3 Hz).
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-methoxy-4-propylphenyl 4-methylbenzenesulfonate (64 mg, 0.2 mmol), the title compound (40 mg; 65%) was prepared as a clear oil, after purification by silica gel chromatography (gradient cyclohexane/dichloromethane).
MS (ES) m/e 305 (M−H)−
NMR1H (CDCl3) δ (ppm): 7.80 (d, 2H, J=8.3 Hz); 7.37 (d, 2H, J=8.1 Hz); 6.85 (s, 1H); 6.71 (d, 1H, J=8.3 Hz); 6.60 (d, 1H, J=8.3 Hz); 6.11 (s, 1H); 2.53 (t, 2H, J=7.6 Hz); 2.50 (s, 3H); 1.63 (se, 2H, J=7.5 Hz); 0.95 (t, 3H, J=7.3 Hz).
To a solution of 2-hydroxy-4-propylphenyl 4-methylbenzenesulfonate (0.11 mmol; 33 mg) under argon, in acetone (0.2 mL), were added K2CO3 (0.13 mmol; 18 mg), NaI (0.02 mmol; 3 mg), and benzylbromide (0.12 mmol; 0.015 mL). The reaction was stirred at 40° C. for 5 hr. The reaction mixture was then hydrolysed with NH4Cl sat. (3 mL) and extracted with ethyl acetate (3*5 mL). Combined organic phases were washed with saturated NaHCO3 (3 mL), dried over MgSO4, concentrated. The residue was purified by preparative TLC (dichlorométhane) to yield the title compound as a clear oil (28 mg; 0.07 mmol; 64%).
MS (ES) m/e 397 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.71 (d, 2H, J=8.1 Hz); 7.34 (m, 5H); 7.12 (d, 3H, J=8.3 Hz); 6.74 (s, 2H); 4.88 (s, 2H); 2.54 (t, 2H, J=7.6 Hz); 2.39 (s, 3H); 1.61 (se, 2H, J=7.4 Hz); 0.92 (t, 3H, J=7.3 Hz).
To a solution of 2-(benzyloxy)-4-propylphenyl 4-methylbenzenesulfonate (0.07 mmol; 28 mg) under argon, in a mixture of ethanol (0.2 mL) and water (0.1 mL), was added KOH (0.09 mmol; 5 mg). The reaction was refluxed for 1 hr, then hydrolysed with NH4Cl sat. (3 mL), and extracted with ethyl acetate (3*5 mL). Combined organic phases were washed with saturated NaHCO3 (3 mL), dried over MgSO4, concentrated. The residue was purified by preparative TLC (cyclohexane/dichlorométhane) to yield the title compound as a clear oil (16 mg; 0.06 mmol; 86%).
MS (ES) m/e 243 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.41 (m, 5H); 6.87 (d, 1H, J=8.0 Hz); 6.79 (s, 1H); 6.71 (d, 1H, J=8.0 Hz); 5.51 (s, 1H); 5.11 (s, 2H); 2.53 (t, 2H, J=7.6 Hz); 1.61 (se, 2H, J=7.5 Hz); 0.94 (t, 3H, J=7.3 Hz).
According to the procedure of example 5(a) except substituting 2,6-difluoropyridine for 2,6-dichlororopyridine (296 mg, 2 mmol), the title compound (450 mg; 81%) was prepared as a clear oil, after purification by silica gel chromatography (gradient cyclohexane/ethyl acetate).
MS (ES) m/e 278 (M+H)+
According to the procedure of example 5(b), except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 2-chloro-6-(2-methoxy-4-propylphenoxy)pyridine (450 mg, 1.62 mmol), the title compound (148 mg; 35%) was prepared as white solid after purification by silica gel chromatography (gradient cyclohexane/ethyl acetate).
MS (ES) m/e 264 (M+H)+
NMR1H (CD3OD) δ (ppm): 7.70 (t, 1H, J=8.0 Hz); 7.06 (d, 1H, J=7.7 Hz); 6.93 (d, 1H, J=8.1 Hz); 6.78 (s, 1H); 6.69 (m, 2H); 2.53 (t, 2H, J=7.8 Hz); 1.65 (se, 2H, J=7.6 Hz); 0.95 (t, 3H, J=7.4 Hz).
According to the procedure of example 5(a) except substituting 2,6-difluoropyridine for 2-amino-6-bromopyridine (173 mg, 1 mmol) the title compound (125 mg; 48%) was prepared as a clear oil, after purification by silica gel chromatography (gradient cyclohexane/dichloromethane).
MS (ES) m/e 259 (M+H)+
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 6-(2-methoxy-4-propylphenoxy)pyridin-2-amine (125 mg, 0.48 mmol), the title compound (5 mg; 4%) was prepared as a clear oil, after preparative TLC (cyclohexane/dichloromethane).
MS (ES) m/e 245 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.45 (t, 1H, J=7.9 Hz); 7.02 (d, 1H, J=8.1 Hz); 6.90 (s, 1H); 6.70 (d, 1H, J=8.0 Hz); 6.27 (d, 1H, J=7.8 Hz); 6.22 (d, 1H, J=7.9 Hz); 4.45 (br, 2H); 2.55 (t, 2H, J=7.6 Hz); 1.66 (se, 2H, J=7.6 Hz); 0.97 (t, 3H, J=7.3 Hz).
According to the procedure of example 4(a), except substituting 4-(2-hydroxyethyl)-2-methoxyphenol for 4-hydroxy-3-methoxybenzaldehyde (304 mg, 2 mmol) the title compound (220 mg; 44%) was prepared as a white solid, after purification by silica gel chromatography (gradient cyclohexane/ethyl acetate).
MS (ES) m/e 248 (M+H)+
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 4-[(6-fluoropyridin-2-yl)oxy]-3-methoxybenzaldehyde (220 mg, 0.89 mmol), the title compound (10 mg; 7%) was prepared as a white solid, after purification by preparative TLC (cyclohexane/ethyl acetate).
MS (ES) m/e 234 (M+H)+
NMR1H (CD3OD) δ (ppm): 9.95 (s, 1H); 7.88 (q, 1H, J1=8.0 Hz); 7.59 (d, 1H, J=2.0 Hz); 7.49 (dd, 1H, J1=8.4 Hz, J2=2.0 Hz); 7.29 (da, 2H, J=8.0 Hz); 6.93 (d, 1H, J=7.6 Hz); 6.75 (dd, 1H, J1=8.0 Hz, J2=2.0 Hz).
According to the procedure of example 4(a), except substituting 4-(2-hydroxyethyl)-2-methoxyphenol for 2-methoxy-4-methylphenol (0.25 mL, 2 mmol) the title compound (457 mg; 97%) was prepared as a white solid, after purification by silica gel chromatography (gradient cyclohexane/dichloromethane).
MS (ES) m/e 234 (M+H)+
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 2-fluoro-6-(2-methoxy-4-methylphenoxy)pyridine (457 mg, 1.93 mmol), the title compound (71 mg; 16%) was prepared as a white solid, after washing with diethyl ether.
MS (ES) m/e 220 (M+H)+
NMR1H (CD3OD) δ (ppm): 7.81 (q, 1H, J1=8.0 Hz); 6.79 (m, 2H); 6.63 (m, 3H); 2.28 (s, 3H).
According to the procedure of example 4(a) except substituting 4-(2-hydroxyethyl)-2-methoxyphenol for 2-methoxy-4-chlorophenol (0.24 mL, 2 mmol) the title compound (423 mg; 84%) was prepared as a white solid, after purification by silica gel chromatography (gradient cyclohexane/dichloromethane).
MS (ES) m/e 254 (M+H)+
To a solution of 2-(4-chloro-2-methoxyphenoxy)-6-fluoropyridine (0.53 mmol; 135 mg) and 4-methylphenylboronic acid (0.94 mmol; 127 mg) in a degased DME/water mixture (1.5/0.5 mL), under argon were added K2CO3 (2.0 mmol; 276 mg), then tetrakis(triphenylphosphine)palladium (0.07 mmol; 47 mg). The reaction was stirred at 105° C. for 48 hr. After concentration, the residue was purified by flash chromatography (gradient cyclohexane/dichloromethane) to yield the desired product along with remaining starting material (160 mg; 0.53 mmol; 100% max).
MS (ES) m/e 310 (M+H)+
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 2-fluoro-6-[(3-methoxy-4′-methyl-1,1′-biphenyl-4-yl)oxy]pyridine (160 mg, 0.53 mmol), the title compound (37 mg; 24%) was prepared as a white solid, after purification by preparative TLC (dichloromethane).
MS (ES) m/e 296 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.81 (q, 1H, J=8.0 Hz); 7.50 (d, 2H, J=8.1 Hz); 7.32 (d, 1H, J=1.6 Hz); 7.27 (d, 2H, J=8.0 Hz); 7.17 (m, 2H); 6.84 (d, 1H, J=8.0 Hz); 6.68 (dd, 1H, J1=7.9 Hz, J2=2.2 Hz); 6.33 (sb, 1H); 2.42 (s, 3H).
To a solution of 5-bromo-2-(2-methoxy-4-propylphenoxy)pyridine (0.19 mmol; 60 mg) under argon, in degased DME (1 mL) were added 3-butyn-1-ol (0.47 mmol; 33 mg), Pd/C (0.02 mmol; 42 mg), CuI (0.04 mmol; 7.6 mg), K2CO3 (0.47 mmol; 64 mg), and triphenylphosphine (0.08 mmol; 21 mg). The reaction mixture was stirred at 80° C. overnight, then filtered on celite, washed with ether (3 mL) then ethyl acetate (3 mL). Combined organic phases were washed with saturated NH4Cl (3 mL), dried over MgSO4, concentrated. The residue was purified by preparative TLC (dichloromethane/ethyl acetate) to yield the desired compound as a clear oil (25 mg; 0.08 mmol; 42%).
MS (ES) m/e 312 (M+H)+
NMR1H (CDCl3) δ (ppm): 8.21 (d, 1H, J=1.8 Hz); 7.67 (dd, 1H, J1=8.6 Hz, J2=2.3 Hz); 7.04 (d, 1H, J=7.9 Hz); 6.82 (m, 3H); 3.81 (t, 2H, J=6.3 Hz); 3.75 (s, 3H); 2.68 (t, 2H, J=6.3 Hz); 2.60 (t, 2H, J=7.8 Hz); 2.07 (sb, 1H); 1.69 (se, 2H, J=7.6 Hz); 0.98 (t, 3H, J=7.4 Hz).
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 4-[6-(2-methoxy-4-propylphenoxy)pyridin-3-yl]but-3-yn-1-ol (25 mg, 0.08 mmol), the title compound (6 mg; 21%) was prepared as a clear oil, after purification by preparative TLC (dichloromethane).
MS (ES) m/e 361 (M+H)+
NMR1H (CDCl3) δ (ppm): 8.24 (s, 1H); 7.75 (d, 1H, J=8.5 Hz); 7.01 (d, 1H, J=8.2 Hz); 6.93 (m, 2H); 6.74 (d, 1H, J=8.1 Hz); 3.54 (t, 2H, J=7.2 Hz); 2.99 (t, 2H, J=7.2 Hz); 2.56 (t, 2H, J=7.8 Hz); 1.66 (se, 2H, J=7.6 Hz); 0.96 (t, 3H, J=7.4 Hz)
The title compound (1 mg; 4%) was isolated from the example 11 (b) as a white solid, after purification by preparative TLC (dichloromethane).
MS (ES) m/e 298 (M+H)+
NMR1H (CDCl3) δ (ppm): 8.25 (s, 1H); 7.75 (d, 1H, J=8.4 Hz); 7.02 (d, 1H, J=8.5 Hz); 6.93 (m, 2H); 6.74 (d, 1H, J=8.0 Hz); 3.84 (t, 2H, J=6.2 Hz); 2.71 (t, 2H, J=6.2 Hz); 2.56 (t, 2H, J=7.9 Hz); 1.66 (se, 2H, J=7.6 Hz); 0.96 (t, 3H, J=7.4 Hz).
According to the procedure of example 4(a) except substituting 4-(2-hydroxyethyl)-2-methoxyphenol for 2-methoxy-4-bromophenol (406 mg, 2 mmol) the title compound compound (540 mg; 90%) was prepared as a clear oil, after purification by silica gel chromatography (gradient cyclohexane/dichloromethane).
MS (ES) m/e 299 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.79 (q, 1H, J=8.0 Hz); 7.16 (m, 2H); 7.06 (d, 1H, J=9.0 Hz); 6.80 (d, 1H, J=8.0 Hz); 6.62 (d, 1H, J=7.8 Hz); 3.81 (s, 3H).
To a suspension of Pd(PPh3)4 (0.025 mmol; 17 mg) under argon, in anhydrous, degased dioxane (2 mL), sheltered from light, were added 2-(4-bromo-2-methoxyphenoxy)-6-fluoropyridine (0.51 mmol; 151 mg), then isobutyl zinc bromide (1.0 mmol; 2.0 mL). The reaction was heated to 105° C. for 24 hr. The mixture was then hydrolysed with water (3 mL), extracted with ethyl acetate (3*3 mL). Combined organic phases were dried over MgSO4, concentrated under reduced pressure. The crude was then purified by preparative chromatography (cyclohexane/dichloromethane) to yield the desired product as a clear oil (28 mg; 0.10 mmol; 20%).
MS (ES) m/e 276 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.71 (q, 1H, J=8.0 Hz); 7.04 (d, 1H, J=7.9 Hz); 6.78 (m, 2H); 6.68 (d, 1H, J=7.3 Hz); 6.56 (d, 1H, J=7.8 Hz); 3.77 (s, 3H); 2.50 (d, 2H, J=7.2 Hz); 1.90 (se, 1H, J=6.7 Hz); 0.96 (d, 6H, J=6.6 Hz).
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 2-fluoro-6-(4-isobutyl-2-methoxyphenoxy)pyridine (25 mg, 0.1 mmol), the title compound (18 mg; 69%) was prepared as a clear oil, without purification.
MS (ES) m/e 262 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.78 (q, 1H, J=8.0 Hz); 7.02 (d, 1H, J=8.2 Hz); 6.89 (s, 1H); 6.77 (d, 1H, J=8.0 Hz); 6.72 (d, 1H, J=8.2 Hz); 6.66 (d, 1H, J=7.9 Hz); 2.46 (d, 2H, J=7.2 Hz); 1.88 (se, 1H, J=6.7 Hz); 0.94 (d, 6H, J=6.6 Hz).
According to the procedure of example 4(a) except substituting 4-(2-hydroxyethyl)-2-methoxyphenol for 4-(hydroxymethyl)-2-methoxyphenol (308 mg; 2 mmol) the title compound (200 mg; 40%) was prepared as a clear oil, after purification by silica gel chromatography (gradient cyclohexane/ethyl acetate).
MS (ES) m/e 250 (M+H)+
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for {4-[(6-fluoropyridin-2-yl)oxy]-3-methoxyphenyl}methanol (104 mg, 0.42 mmol), the title compound (98 mg; 98%) was prepared as a white solid, after washing with diethyl ether.
MS (ES) m/e 236 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.81 (q, 1H, J=8.0 Hz); 7.11 (s, 1H); 7.08 (d, 1H, J=8.3 Hz); 6.95 (d, 1H, J=8.3 Hz); 6.83 (d, 1H, J=7.9 Hz); 6.68 (d, 1H, J=7.9 Hz); 4.46 (s, 2H).
To a solution of 2-[(6-fluoropyridin-2-yl)oxy]-5-(hydroxymethyl)phenol (0.42 mmol; 104 mg) under argon, in anhydrous DMF (0.8 mL), were added K2CO3 (0.5 mmol; 68 mg), DMAP (0.08 mmol; 12 mg), and acetic anhydride (0.41 mmol; 0.04 mL). The reaction was stirred at room temperature overnight. After dilution with ethyl acetate (4 mL), the organic phase was washed with saturated NaHCO3 (3*3 mL), dried (MgSO4), concentrated in vacuo, purified by preparative TLC (dichlorométhane) to yield the title compound as a clear oil (3 mg; 0.01 mmol; 3%).
MS (ES) m/e 278 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.82 (q, 1H, J=8.0 Hz); 7.56 (m, 3H); 6.82 (d, 1H, J=6.9 Hz); 6.68 (dd, 1H, J1=7.8 Hz, J2=2.6 Hz); 5.16 (s, 2H); 2.17 (s, 3H).
A mixture containing 2-methoxy-4-propylphenol (0.625 mmol; 100 μl), copper(II) acetate (0.625 mmol; 114 mg), 4-methoxyphenylboronic acid (1.25 mmol; 190 mg), triethylamine (3.12 mmol; 0.43 ml), some crushed molecular sieves 4 Å in dichloromethane (3 ml) was stirred at rt under air for 24 h. The residue is filtered with chloroform on Celite. The organic phase is washed with saturated NH4Cl, saturated NaHCO3 and brine. After drying (MgSO4), concentration and purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—20/80), the title compound is collected as a colorless oil (70 mg; 0.26 mmol; 41%).
MS (ES) 273 [M+1]+ and 295 [M+Na]+
NMR1H (CDCl3) δ (ppm): 6.94 (d, 2H, J=9.1 Hz); 6.85 (d, 2H, J=9.1 Hz); 6.82 (s, 1H); 6.80 (d, 1H, J=8.1 Hz); 6.70 (d, 1H, J=8.2 Hz); 3.87 (s, 3H); 3.80 (s, 3H); 2.58 (t, 2H, J=7.7 Hz); 1.67 (se, 2H, J=7.6 Hz); 0.98 (t, 3H, J=7.3 Hz).
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 2-methoxy-1-(4-methoxyphenoxy)-4-propylbenzene (0.18 mmol; 50 mg) and adding 4 equivalents (0.735 mmol; 735 μl) of boron tribromide, the title compound was prepared in 32% yield (0.06 mmol; 15 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—20/80).
MS (ES) 257 [M−1]−
NMR1H (CDCl3) δ (ppm): 6.99 (d, 2H, J=9.0 Hz); 6.89 (d, 2H, J=9.0 Hz); 6.87 (s, 1H); 6.72 (d, 1H, J=8.2 Hz); 6.63 (d, 1H, J=8.1 Hz); 5.57 (s br, 1H); 3.82 (s, 3H); 2.54 (t, 2H, J=7.8 Hz); 1.64 (se, 2H, J=7.5 Hz); 0.96 (t, 3H, J=7.3 Hz). NOE observed between δ 3.82 and 6.89 ppm.
According to the procedure of example 16(a) except substituting 4-methoxyphenylboronic acid for 3-acetamidophenylboronic acid (1.25 mmol; 224 mg) the title compound was prepared in 10% yield (0.06 mmol; 18 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—70/30).
NMR1H (CDCl3) δ (ppm): 7.28-7.16 (m, 3H); 7.05 (s, 1H); 6.92 (d, 1H, J=8.0 Hz); 6.83 (s, 1H); 6.76 (d, 1H, J=7.9 Hz); 6.68 (d, 1H, J=7.4 Hz); 3.82 (s, 3H); 2.60 (t, 2H, J=7.4 Hz); 2.15 (s, 3H); 1.68 (t, 3H, J=7.4 Hz).
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for N-[3-(2-methoxy-4-propylphenoxy)phenyl]acetamide (0.06 mmol; 17 mg), the title compound was prepared in 56% yield (0.03 mmol; 9 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—70/30).
MS (ES) 286 [M+1]+ and 308 [M+Na]+
NMR1H (DMSO) δ (ppm): 9.90 (s, 1H); 9.37 (s, 1H); 7.28-7.19 (m, 3H); 6.86 (d, 1H, J=8.1 Hz); 6.79 (s, 1H); 6.64 (d, 1H, J=8.1 Hz); 6.52 (d, 1H, J=7.9 Hz); 2.00 (s, 3H); 1.59 (se, 2H, J=7.5 Hz); 0.92 (t, 3H, J=7.3 Hz).
To 2-(4-ethyl-2-methoxyphenoxy)-6-fluoropyridine (94 mg; 0.32 mmol), under argon, was added butylamine (0.5 mL). The reaction was heated to 80° C. for 18 hours. The mixture was concentrated in vacuo. After quenching with saturated NaHCO3 (10 mL), extractions with dichloromethane (3*5 mL), the organic phase was dried over NaSO4, and concentrated in vacuo to give the title compound as a light brown oil used without further purification (87 mg; 0.29 mmol; 89%).
MS (ES) m/e 301 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for N-butyl-6-(4-ethyl-2-methoxyphenoxy)pyridin-2-amine (87 mg; 0.29 mmol), the title compound(36 mg; 43%) was obtained as a light brown oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 8/2)
MS (ES) m/e 287 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.41 (t, 1H, J=7.9 Hz); 7.01 (d, 1H, J=8.1 Hz); 6.91 (s, 1H); 6.69 (d, 1H, J=8.0 Hz); 6.17 (d, 1H, J=7.8 Hz); 6.06 (d, 1H, J=8.1 Hz); 4.56 (sl, 1H); 3.18 (t, 2H, J=7.0 Hz); 2.61 (q, 2H, J=7.5 Hz); 1.55 (qt, 2H, J=7.5 Hz); 1.39 (se, 2H, J=7.4 Hz); 1.23 (t, 3H, J=7.6 Hz); 0.93 (t, 3H, J=7.3 Hz).
To a solution of sodium (55 mg; 2.39 mmol), under argon, in ethanol (2 mL), was added 2-(4-ethyl-2-methoxyphenoxy)-6-fluoropyridine (82 mg; 0.33 mmol). The reaction was heated to 80° C. for 16 hours then to 90° C. for 26 hours. The mixture was concentrated in vacuo. After quenching with saturated NaHCO3 (10 mL), extractions with ethyl acetate (3*5 mL), the organic phase was dried over NaSO4, and concentrated in vacuo to give the desired product as a light brown oil used without further purification (82 mg; 0.30 mmol; 90%).
MS (ES) m/e 274 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-ethoxy-6-(4-ethyl-2-methoxyphenoxy)pyridine (82 mg; 0.30 mmol), the title compound (31 mg; 37%) was prepared as a light brown oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 8/2).
MS (ES) m/e 260 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.56 (t, 1H, J=7.6 Hz); 7.01 (d, 1H, J=8.2 Hz); 6.91 (d, 1H, J=1.8 Hz); 6.70 (dd, 1H, J1=1.9 Hz, J2=8.2 Hz); 6.46 (d, 1H, J=5.1 Hz); 6.43 (d, 1H, J=4.8 Hz); 4.22 (q, 2H, J=7.0 Hz); 2.61 (q, 2H, J=7.6 Hz); 1.33 (t, 3H, J=7.1 Hz); 1.23 (t, 3H, J=7.0 Hz).
To a suspension of K2CO3 (2 mmol; 276 mg) in anhydrous acetonitrile (1 mL) under argon, was added 2-methoxy-4-ethylphenol (0.285 mL; 2 mmol) followed by 1-fluoro-4-nitro-2-(trifluoromethyl)benzene (418 mg; 2 mmol). The reaction mixture was stirred at 80° C. overnight. Concentrated under argon, washed with NaOH (0.1N; 3 mL), the mixture was extracted with ethyl acetate (2*3 mL). Combined organic phases were dried over MgSO4, concentrated in vacuo, to give the title product as a light brown oil (651 mg; 95%), used without further purification.
MS (ES) m/e 342 (M+H)+.
4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene (1.90 mmol; 651 mg) was dissolved in anhydrous THF (8 mL) under argon. Palladium on charcoal (0.095 mmol; 20 mg) was added and the reaction was flushed twice with hydrogen, then left to stir overnight. The reaction mixture was filtered on celite, rinsed with methanol (3*10 mL). Concentration yielded a light brown oil (579 mg; 98%) used without further purification.
MS (ES) m/e 312 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-2-methoxyphenoxy)-3-(trifluoromethyl)aniline (54 mg; 0.170 mmol), the title compound (24 mg; 47%) was prepared as a light brown solid, after purification by preparative TLC (dichloromethane/methanol: 98/2).
MS (ES) m/e 298 (M+H)+
1H NMR (CDCl3) δ (ppm): 6.95 (d, 1H, J=2.1 Hz); 6.88 (s, 1H); 6.81 (d, 1H, J=8.7 Hz); 6.75 (dd, 1H, J1=2.2 Hz, J2=8.4 Hz); 6.70 (d, 1H, J=8.2 Hz); 6.64 (d, 1H, 8.0 Hz); 2.59 (q, 2H, J=7.6 Hz); 1.22 (t, 3H, 7.6 Hz).
According to the procedure of example 20(a), except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 3-bromo-2-nitropyridine (2 mmol; 406 mg), the title compound (73 mg; 13%) was prepared after chromatography on silica gel (gradient cyclohexane/ethyl acetate).
MS (ES) m/e 275 (M+H)+
Alternatively 3-(4-ethyl-2-methoxyphenoxy)-2-nitropyridine can be synthezized using the following procedure:
To a stirred solution of 3-Amino 2-nitro pyridine (2.5 g, 17.97 mmol) in dry ethanol (20 ml) was added 10 ml of tetrafluoroboric acid (48% in water). The reaction mixture was cooled to 0° C. and isoamyl nitrite (2.6 g, 22.4 mmol) was added dropwise at 0° C. and stirred at 0° C. for 1 hour. The reaction mixture was filtered, and the solid obtained was washed with diethyl ether. The filtered solid was added to preheated (150 mL) toluene with stirring and reaction mixture was refluxed for 24 hours. The solvent was evaporated and the residue taken in ethyl acetate (200 ml) and washed with water followed by brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the crude 3-fluoro-2-nitropyridine. This was purified by column over silica gel using 10% ethyl acetate in pet ether as eluant to get 1 g (39%) of the title compound as a yellow solid.
1H NMR (CDCl3), δ (ppm): 8.45 (d, J=4.24 Hz, 1H), 7.78-7.83 (m, 1H), 7.70-7.74 (m, 1H)
To a stirred solution of 3-Fluoro 2-nitro pyridine (1.6 g, 0.01126 mol) in dry Acetonitrile (20 ml) was added 4-Ethyl-2-methoxy phenol (1.71 g, 11.3 mmol) in dry acetonitrile (10 ml) followed by potassium hydroxide (0.696 g, 12.4 mmol). The reaction mixture was heated to 80° C. and maintained for 2 hours. The solvent was evaporated and taken in ethyl acetate (200 ml). The organic layer was washed with water followed by brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 2.6 g of crude product purified by column chromatography (5% Ethyl acetate in Petroleum ether) to yield: 1.75 g (56%) of title compound.
To a stirred solution of 3-(4-ethyl-2-methoxyphenoxy)-2-nitropyridine (1.3 g, 4.7 mmol) in methanol (30 ml) were added anhydrous Ferric chloride (66 mg) and activated charcoal (66 mg). The resulting mixture was heated to reflux and Hydrazine hydrate (80%) (2 mL, 39 mmol) was added dropwise. The reaction was allowed to stir under reflux condition for 5 hours, then filtered through celite. The filtrate was concentrated under reduced pressure, taken in ethyl acetate (150 ml). The organic phase was washed with water followed by brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 1.11 g of the title compound, 100% yield.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 3-(4-ethyl-2-methoxyphenoxy)pyridin-2-amine (63 mg; 0.26 mmol) the title compound (13 mg; 22%) was obtained as a light brown oil, after two purifications by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 231 (M+H)+
1H NMR (MeOD) δ (ppm): 7.61 (m, 1H); 6.84 (m, 3H); 6.70 (d, 1H, J=8.2 Hz); 6.55 (m, 1H); 2.60 (q, 2H, J=7.5 Hz); 1.23 (t, 3H, J=7.6 Hz)
According to the procedure of example 20(a), except substituting 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 5-bromo-2-nitropyridine (406 mg, 2 mmol), the title compound (220 mg; 38%) was prepared as a white solid, after chromatography on silica gel (gradient cyclohexane/dichloromethane), along with 5-bromo-2-(2-methoxy-4-propylphenoxy)pyridine (238 mg; 37%).
MS (ES) m/e 289 (M+H)+
According to the procedure of example 20(b), except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 5-(2-methoxy-4-propylphenoxy)-2-nitropyridine (144 mg; 0.5 mmol), the title compound (130 mg; 100%) was prepared as a white solid, without purification.
MS (ES) m/e 259 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-[(6-aminopyridin-3-yl)oxy]-5-propylphenol (130 mg, 0.50 mmol), the title compound (112 mg, 92%) was prepared as a white solid after washing with diethyl ether.
MS (ES) m/e 245 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.92 (s, 1H); 7.22 (d, 1H, J=8.8 Hz); 6.90 (s, 1H); 6.68 (q, 2H, J=9.3 Hz); 6.54 (d, 1H, J=8.8 Hz); 2.55 (t, 2H, J=7.7 Hz); 1.66 (se, 2H, J=7.4 Hz); 0.97 (t, 3H, J=7.3 Hz).
To a solution of 2-[(6-aminopyridin-3-yl)oxy]-5-propylphenol (0.12 mmol; 30 mg) under argon, in anhydrous dichlorométhane (0.5 mL), cooled to −40° C., were added pyridine (0.13 mmol; 0.01 mL) and MsCl (0.12 mmol; 0.01 mL). The reaction mixture was stirred overnight while progressively heating to room temperature. After quenching with NH4Cl (1 mL), extraction with ethyl acetate (3*3 mL), combined organic phases were washed with water (3 mL), dried over MgSO4, concentrated in vacuo. The crude was purified by preparative TLC (dichloromethane/ethyl acetate) to yield the title compound as a white solid (37 mg; 0.09 mmol; 77%).
MS (ES) m/e 401 (M+H)+
1H NMR (acetone-d6) δ (ppm): 8.16 (s, 1H); 7.52 (d, 1H, J=8.7 Hz); 7.33 (s, 1H); 7.22 (t, 2H, J=8.5 Hz); 7.04 (d, 1H, J=7.7 Hz); 3.35 (s, 3H); 3.28 (s, 3H); 2.63 (m, 2H); 1.67 (m, 2H); 0.95 (m, 3H).
To a solution of 2-({6-[(methylsulfonyl)amino]pyridin-3-yl}oxy)-5-propylphenyl methanesulfonate (0.09 mmol; 30 mg), under argon, in water (0.5 mL), was added KOH (0.26 mmol; 15 mg). The reaction mixture was refluxed for 4 hr. After quenching with NH4Cl (1 mL), extraction with ethyl acetate (3*3 mL), combined organic phases were washed with water (3 mL), dried over MgSO4, concentrated in vacuo, to yield the title compound as a white solid (37 mg; 0.09 mmol; 77%).
MS (ES) m/e 323 (M+H)+
1H NMR (acetone-d6) δ (ppm): 7.99 (d, 1H, J=13.2 Hz); 7.31 (d, 1H, J=9.1 Hz); 7.16 (d, 1H, J=9.0 Hz); 6.94 (d, 1H, J=7.8 Hz); 6.89 (s, 1H); 6.73 (d, 1H, J=7.3 Hz); 3.24 (s, 3H); 2.80 (s, 3H); 2.54 (t, 2H, J=6.8 Hz); 1.64 (se, 2H, J=6.4 Hz); 0.95 (t, 3, J=6.3 Hz).
To a solution of 2-[(6-aminopyridin-3-yl)oxy]-5-propylphenol (0.20 mmol; 50 mg) under argon, in H2SO4 (35%; 0.2 mL), cooled to 0° C., was slowly added NaNO2 (0.26 mmol; 18 mg) in water (0.2 mL). After 30 min, CuSO4 (3 mmol; 477 mg) in water (1 mL), then Cu2O (0.18 mmol; 26 mg) were added. After 30 min, the mixture was neutralised with NaHCO3 sat. (1 mL), extracted with ethyl acetate (3*3 mL). Combined organic phases were washed with water (3 mL), dried over MgSO4, concentrated in vacuo. An analytical sample was obtained by preparative TLC to yield the title compound as a white solid (5 mg; 0.02 mmol; ca 20%).
MS (ES) m/e 246 (M+H)+
1H RMN (CD3OD) δ (ppm): 7.48 (dd, 1H, J1=9.8 Hz, J2=3.2 Hz); 7.01 (d, 1H, J=3.1 Hz); 6.80 (d, 1H, J=8.2 Hz); 6.76 (d, 1H, J=1.9 Hz); 6.63 (dd, 1H, J1=8.1 Hz, J2=2.0 Hz); 6.54 (d, 1H, J=9.8 Hz); 2.48 (t, 2H, J=7.8 Hz); 1.60 (se, 2H, J=7.5 Hz); 0.91 (t, 3H, J=7.4 Hz).
To a solution of 5-(2-hydroxy-4-propylphenoxy)pyridin-2-ol (0.08 mmol; 20 mg) under argon, in anhydrous DMF (0.5 mL) cooled to 0° C., were added LiOH (0.09 mmol; 2 mg), then EtBr (0.09 mmol; 0.007 mL). After allowing the mixture to warm overnight up to room temperature, the reaction was neutralised with NaHCO3 (1 mL), extracted with ethyl acetate (3*3 mL). Combined organic phases were washed with water (3 mL), dried over MgSO4, concentrated in vacuo to yield the title compound as a brown oil (14 mg; 0.05 mmol; 58%), used as such.
MS (ES) m/e 302 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 5-(2-ethoxy-4-propylphenoxy)-1-ethylpyridin-2(1H)-one(14 mg; 0.05 mmol), the title compound (7 mg; 51%) was prepared as a white solid, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 274 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.23 (d, 1H, J=6.8 Hz); 7.10 (s, 1H); 6.86 (s, 1H); 6.69 (d, 1H, J=8.0 Hz); 6.63 (d, 1H, J=8.0 Hz); 6.58 (d, 1H, J=9.8 Hz); 3.95 (q, 2H, J=7.1 Hz); 2.51 (t, 2H, J=7.7 Hz); 1.62 (se, 2H, J=7.8 Hz); 1.34 (t, 3H, J=7.2 Hz); 0.92 (t, 3H, J=7.3 Hz).
According to the procedure of example 5(a) except substituting 2,6-difluoropyridine for 2,4,6-trifluoropyridine (0.32 mL, 2 mmol), the title compounds (265 mg; 47%) were prepared together as a clear oil, after purification by silica gel chromatography (gradient cyclohexane/dichloromethane).
MS (ES) m/e 280 (M+H)+
According to the procedure of example 5(b), except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 2,4-difluoro-6-(2-methoxy-4-propylphenoxy)pyridine and 2,6-difluoro-4-(2-methoxy-4-propylphenoxy)pyridine (67 mg, 0.24 mmol), title compound A, as a white solid (11 mg; 17%), and title compound B as a clear oil (22 mg; 35%) were prepared after purification by preparative TLC (dichloromethane/ethyl acetate).
A: MS (ES) m/e 266 (M+H)+
NMR1H (CDCl3) δ (ppm): 7.01 (d, 1H, J=8.2 Hz); 6.92 (s, 1H); 6.77 (d, 1H, J=8.3 Hz); 6.49 (d, 1H, J=8.7 Hz); 6.41 (d, 1H, J=7.7 Hz); 5.72 (br, 1H); 2.57 (t, 2H, J=7.8 Hz); 1.67 (se, 2H, J=7.3 Hz); 0.97 (t, 3H, J=7.3 Hz).
B: MS (ES) m/e 266 (M+H)+
NMR1H (CDCl3) δ (ppm): 6.97 (d, 1H, J=8.2 Hz); 6.92 (s, 1H); 6.80 (d, 1H, J=8.3 Hz); 6.36 (s, 2H); 5.37 (br, 1H); 2.58 (t, 2H, J=7.8 Hz); 1.68 (se, 2H, J=7.6 Hz); 0.97 (t, 3H, J=7.4 Hz).
To a solution of 4-[(6-fluoropyridin-2-yl)oxy]-3-methoxy benzaldehyde (300 mg; 1.2 mmol) with trifluoro methyltrimethylsilane (228 μl; 1.46 mmol) in THF (3 ml) under argon at 0° C. was added a molar solution of TBAF in THF (10 μl; 0.012 mmol). The reaction mixture was allowed to stir at rt for 2 h and a molar aqueous solution of HCl was added dropwise (2.5 ml; 2.5 mmol). The reaction mixture was stirred for another 2 h. water and diethylether were added. The aqueous phase was further extracted (2×EtOAc). Combined organic phases were dried over MgSO4, concentrated in vacuo to afford the title compound as a white solid (333 mg; 1.05 mmol; 88%).
1H NMR (CDCl3) δ (ppm): 7.79 (q, 1H, J=8.0 Hz); 7.24-7.20 (m, 2H); 7.17-7.09 (m, 1H); 6.81 (d, 1H, J=8.0 Hz); 6.64 (d, 1H, J=7.8 Hz); 5.10 (m, 1H); 3.85 (s, 3H).
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine by 2,2,2-trifluoro-1-{4-[(6-fluoropyridin-2-yl)oxy]-3 methoxyphenyl}ethanol (0.15 mmol; 50 mg) and adding 3.5 equivalents (0.47 mmol; 470 μl) of boron tribromide, the title compound was prepared in 84% yield (0.13 mmol; 38 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—40/60).
MS (ES) 304 [M+1]+
1H NMR (DMSO) δ (ppm): 9.79 (s, 1H); 7.97 (q, 1H, J=8.3 Hz); 7.12 (s, 1H); 7.11 (d, 1H, J=8.1 Hz); 6.96 (d, 1H, J=9.1 Hz); 6.85 (d, 1H, J=8.0 Hz); 6.81 (d, 2H, J=5.4 Hz); 5.11 (qt, 1H).
To a solution of 2,2,2-trifluoro-1-{4-[(6-fluoropyridin-2-yl)oxy]-3-methoxyphenyl}ethanol (0.52 mmol; 165 mg), tosyl chloride (0.57 mmol; 109 mg) and DMAP (0.01 mmol; 1.5 mg) under argon in dichloromethane (4 mL) at 0° C. was added TEA (1.04 mmol; 145 μl). The reaction mixture was stirred at rt for 3 h, then washed with brine (2×), dried over MgSO4, concentrated and purified by preparative TLC on silica gel (ethyl acetate/cyclohexane—30/70) to yield the title compound (101 mg; 0.21 mmol; 41%).
1H NMR (CDCl3) δ (ppm): 7.78 (q, 1H, J=8.6 Hz); 7.65 (d, 2H, J=8.2 Hz); 7.29 (d, 2H, J=8.6 Hz); 7.06 (d, 1H, J=8.2 Hz); 6.92 (d, 1H, J=9.7 Hz); 6.86 (s, 1H); 6.77 (d, 1H, J=8.0 Hz); 6.63 (d, 1H, J=8.1 Hz); 5.69 (q, 1H, J=6.3 Hz); 3.67 (s, 3H); 2.40 (s, 3H).
A solution of 2,2,2-trifluoro-1-{4-[(6-fluoropyridin-2-yl)oxy]-3-methoxyphenyl}ethyl 4-methylbenzenesulfonate (0.2 mmol; 96 mg) in ethanol (3 ml) containing a catalytic amount of Pd/C (10% wet; 0.014 mmol; 30 mg) was stirred for 16 h at rt under 2.5 atm of hydrogen. Purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—30/70) afforded the title compound (48 mg; 0.16 mmol; 80%).
MS (ES) 302 [M+1]+
1H NMR (CDCl3) δ (ppm): 7.75 (q, 1H, J=7.9 Hz); 7.13 (d, 1H, J=8.5 Hz); 6.96-6.90 (m, 2H); 6.76 (d, 1H, J=7.3 Hz); 6.59 (d, 1H, J=7.9 Hz); 3.80 (s, 3H); 3.40 (q, 1H, J=10.9 Hz).
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine by 2-fluoro-6-[2-methoxy-4-(2,2,2-trifluoroethyl)phenoxy]pyridine (0.14 mmol; 43 mg) and adding 3.5 equivalents (0.5 mmol; 500 μl) of boron tribromide, the title compound was prepared in 75% yield (0.11 mmol; 30 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—30/70).
MS (ES) 288 [M+1]+
1H NMR (CDCl3) δ (ppm): 7.84 (q, 1H, J=7.6 Hz); 7.12 (d, 1H, J=8.7 Hz); 7.05 (s, 1H); 6.89-6.82 (m, 2H); 6.71 (d, 1H, J=6.3 Hz); 6.02 (s br, 1H); 3.36 (q, 1H, J=10.3 Hz).
To a solution of 2,2,2-trifluoro-1-{4-[(6-fluoropyridin-2-yl)oxy]-3-methoxyphenyl}ethanol (0.22 mmol; 70 mg) under argon in dichloromethane (2 mL) at −78° C. was added dropwise DAST (0.22 mmol; 29 μl). The reaction mixture was let come back to rt for 2 h and quenched with brine (3 ml). The aqueous phase was collected, neutralized with sodium bicarbonate and extracted twice with chloroform. The organic phases were combined, dried over MgSO4, concentrated and purified by preparative TLC on silica gel (ethyl acetate/cyclohexane—30/70) to yield the title compound (25 mg; 0.08 mmol; 37%).
1H NMR (CDCl3) δ (ppm): 7.78 (q, 1H, J=8.1 Hz); 7.22 (d, 1H, J=8.0 Hz); 7.10 (m, 2H); 6.80 (d, 1H, J=8.0 Hz); 6.62 (d, 1H, J=7.8 Hz); 5.62 (dq, 1H, J=37.8 and 6.2 Hz); 3.82 (s, 3H).
To a solution of 2-fluoro-6-[2-methoxy-4-(1,2,2,2-tetrafluoroethyl)phenoxy]pyridine (0.078 mmol; 25 mg) under argon in THF (1 mL) at 0° C. was added dropwise a one molar solution of LiHMDS in THF (0.094 mmol; 94 μl). The reaction mixture was let come back to rt for 16 h. Concentration and purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—30/70) afforded the title compound (10 mg; 0.033 mmol; 43%).
1H NMR (CDCl3) δ (ppm): 7.73 (q, 1H, J=7.9 Hz); 7.21 (d, 1H, J=8.1 Hz); 7.12 (d, 1H, J=9.9 Hz); 7.11 (s, 1H); 6.80 (d, 1H, J=7.9 Hz); 6.61 (d, 1H, J=7.7 Hz); 3.81 (s, 3H).
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine by 2-fluoro-6-[2-methoxy-4-(trifluorovinyl)phenoxy]pyridine (0.033 mmol; 10 mg) and adding 3.5 equivalents (0.117 mmol; 117 μl) of boron tribromide, the title compound was prepared in 64% yield (0.021 mmol; 6 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—30/70).
1H NMR (CDCl3) δ (ppm): 7.76 (q, 1H, J=8.0 Hz); 7.13 (d, 1H, J=1.9 Hz); 7.11 (d, 1H, J=8.6 Hz); 6.98 (d, 1H, J=10.0 Hz); 6.80 (d, 1H, J=8.0 Hz); 6.63 (d, 1H, J=9.6 Hz); 6.00 (s br, 1H).
According to the procedure of example 4(a) except substituting 2,6-Difluoropyridine for 1-(3,4-difluorophenyl)ethanone (0.77 mmol; 0.97 ml), the title compound was isolated as a light brown oil (244 mg; quantitative) used without purification.
MS (ES) m/e 289 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 1-[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]ethanone (244 mg; 0.70 mmol), an analytical sample of the title compound (11 mg; 5%) was prepared as a light brown oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 275 (M+H)+
1H NMR (CDCl3) δ (ppm): 9.38 (dd, 1H, J1=2.0 Hz, J2=11.6 Hz); 7.65 (d, 1H, J=8.4 Hz); 6.95 (t, 2H, J=8.0 Hz); 6.85 (d, 1H, J=8.1 Hz); 6.72 (d, 1H, J=8.0 Hz); 5.59 (sl, 1H); 2.62 (q, 2H, J=7.6 Hz); 2.56 (s, 3H); 1.24 (t, 3H, J=7.5 Hz).
To a solution of 1-[4-(4-ethyl-2-hydroxyphenoxy)-3-fluorophenyl]ethanone (46 mg; 0.17 mmol), under argon, in ethanol (1 mL), was added O-methylhydroxylamine hydrochloride (14 mg; 0.17 mmol) and 0.05 mL of triethylamine. The reaction was stirred to room temperature overnight. The mixture was concentrated in vacuo to give the desired product as light brown oil after purification by preparative TLC (14.5 mg; 0.048 mmol; 28%).
1H NMR (CDCl3) δ (ppm): 7.53 (dd, 1H, J1=1.9 Hz, J2=12.0 Hz); 7.33 (d, 1H, J=8.5 Hz); 6.99 (t, 1H, J=8.5 Hz); 6.90 (d, 1H, J=1.5 Hz); 6.75 (d, 1H, J=8.3 Hz); 6.66 (dd, 1H, J1=1.4 Hz, J2=8.2 Hz); 5.54 (s, 1H); 3.99 (s, 3H); 2.60 (q, 2H, J=7.6 Hz); 2.19 (s, 3H); 1.23 (t, 3H, J=7.6 Hz).
To a solution of {4-[(6-fluoropyridin-2-yl)oxy]-3-methoxyphenyl}methanol (367 mg; 1.47 mmol), under argon, in dichloromethane (6 mL), cooled to −40° C., was added pyridine (131 μL; 1.62 mmol) then methanesulfonyl chloride (115 μL; 1.47 mmol). The reaction mixture was allowed to stir for 6 hr, with gradual warming to room temperature. The mixture was cooled to −40° C., pyridine (50 μL; 0.62 mmol) and methanesulfonyl chloride (40 μL; 0.51 mmol) were added. The reaction was stirred overnight, with gradual warming to room temperature.
The reaction was hydrolysed with saturated NH4Cl (10 mL), extracted with ethyl acetate (2*5 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (185 mg; 47%) was obtained as a light oil, after purification on silica gel (cyclohexane/ethyl acetate: 95/5).
1H NMR (CDCl3) δ (ppm): 7.75 (q, 1H, J=7.6 Hz); 7.10 (d, 1H, J=7.9 Hz); 7.04 (s, 1H); 7.00 (d, 1H, J=8.1 Hz); 6.74 (d, 1H, J=7.9 Hz); 6.57 (dd, 1H, J1=7.8 Hz, J2=1.8 Hz); 4.60 (s, 2H); 3.79 (s, 3H).
To a solution of imidazole (18 mg; 0.27 mmol) and NaH (12 mg; 0.30 mmol) in DMF (1 mL), under argon, was added a solution of 2-[4-(chloromethyl)-2-methoxyphenoxy]-6-fluoropyridine (65 mg; 0.24 mmol) in DMF (1 mL). The reaction mixture was allowed to stir overnight, to 40° C. After concentration, the reaction was hydrolysed with saturated NH4Cl (1 mL), extracted with AcOEt (2*1 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, the title compound (68 mg; 93%) was obtained.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-fluoro-6-[4-(1H-imidazol-1-ylmethyl)-2-methoxy phenoxy]pyridine (68 mg; 0.23 mmol), the title compound (16 mg; 24%) was obtained as a white solid, after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 286 (M+H)+
1H NMR (MeOD) δ (ppm): 7.93 (m, 2H); 7.28 (sl, 1H); 7.12 (m, 2H); 6.84 (m, 3H); 6.72 (dd, 1H, J1=7.8 Hz, J2=2.0 Hz); 5.27 (s, 2H).
To a solution of triazole (18 mg; 0.267 mmol) and NaH (10 mg; 0.25 mmol) in DMF (1 mL), under argon, was added a solution of 2-[4-(chloromethyl)-2-methoxyphenoxy]-6-fluoropyridine (65 mg; 0.243 mmol) in DMF (1 mL). The reaction mixture was allowed to stir overnight at 40° C. After concentration, the reaction was hydrolysed with saturated NH4Cl (1 mL), extracted with AcOEt (2*1 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, the title compound (72 mg; quantitative) was obtained.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 2-fluoro-6-[2-methoxy-4-(1H-1,2,4-triazol-1-ylmethyl)phenoxy]pyridine (71 mg; 0.24 mmol), the title compound was prepared (37 mg; 54%) after purification by preparative TLC on silica gel (dichloromethane/methanol—9/1).
1H NMR (MeOD) δ (ppm): 8.75 (s, 1H); 8.08 (s, 1H); 7.74 (q, 1H, J=7.7 Hz); 6.95 (d, 1H, J=8.2 Hz); 6.82 (d, 1H, J=1.8 Hz); 6.76 (dd, 1H, J1=8.1 Hz, J2=1.8 Hz); 6.64 (dd, 1H, J1=8.0 Hz, J2=1.0 Hz); 6.55 (dd, 1H, J1=7.8 Hz, J2=2.2 Hz); 5.32 (s, 2H).
To a solution of 5-Ethyl-2-(6-fluoro-pyridin-2-yloxy)-phenol (20 mg; 0.09 mmol), under argon, in dimethylformamide (2 mL), cooled to 0° C., was added triethylamine (36 μL; 0.26 mmol) and acetic acid (10 μL; 0.18 mmol). The reaction mixture was allowed to stir overnight, with gradual warming to roomtemperature. The reaction was concentrated, diluted with saturated NaHCO3 (5 mL) and extracted with ethyl acetate (3*3 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, the title compound (8 mg; 34%) was obtained as clear oil, after purification on neutral alumina gel (cyclohexane/ethyl acetate: 9/1).
1H RMN (CDCl3) (ppm): 7.73 (q, 1H, J=8.0 Hz); 7.11 (m, 2H); 6.72 (d, 1H, J=8.0 Hz); 6.60 (dd, 1H, J1=7.8 Hz, J2=2.4 Hz); 2.67 (q, 2H, J=7.6 Hz); 2.11 (s, 3H); 1.26 (t, 3H, J=7.6 Hz).
According to the procedure of example 21 (a3) except substituting 3-Fluoro 2-nitro pyridine by 2-fluoronitrobenzene (0.72 mmol; 102 mg), the title compound was prepared in quantitative yield (205 mg) and used without further purification.
MS (ES) m/e 274 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene by 4-ethyl-2-methoxy-1-(2-nitrophenoxy)benzene (0.66 mmol; 180 mg) and THF by ethanol, the title compound was prepared in quantitative yield (181 mg) and used without further purification.
MS (ES) m/e 244 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 2-(4-ethyl-2-methoxyphenoxy)aniline (50 mg; 0.21 mmol), the title compound was prepared in 42% yield (0.09 mmol; 20 mg) after purification by preparative TLC on silica gel (dichloromethane/methanol—40/60).
MS (ES) m/e 244 (M+H)+
1H RMN (CDCl3) δ (ppm): 6.93 (t, 1H, J=7.4 Hz); 6.89-6.85 (m, 2H); 6.82-6.79 (m, 2H); 6.76-6.72 (m, 1H) 6.64 (dd, 1H, J1=8.1 Hz; J2=1.8 Hz); 2.58 (q, 2H, J=7.6 Hz); 1.22 (t, 3H, J=7.6 Hz).
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 2-[4-(chloromethyl)-2-methoxyphenoxy]-6-fluoro pyridine (205 mg; 0.77 mmol), the title compound (185 mg; 95%) was prepared as a light brown solid without further purification.
MS (ES) m/e 254 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.81 (q, 1H, J=8.0 Hz); 7.11 (m, 2H); 6.95 (dd, 1H, J1=8.2 Hz, J2=1.9 Hz); 6.83 (d, 1H, J=8.0 Hz); 6.68 (dd, 1H, J1=7.9 Hz, J2=2.1 Hz); 4.55 (s, 2H).
To a solution of 5-(chloromethyl)-2-[(6-fluoropyridin-2-yl)oxy]phenol (50 mg; 0.20 mmol), under argon, in methanol (1 mL) was added sodium methoxylate (3.94 mmol; 22 mg) and sodium iodide (0.07 mmol; 10 mg). The reaction mixture was allowed to stir at room temperature overnight. The reaction was hydrolysed with saturated NH4Cl (5 mL), extracted with ethyl acetate (3*2 mL), and washed with 5 mL of satured NaHCO3. Combined organic phases were dried over Na2SO4, concentrated in vacuo, the title compound (49 mg; 100%) was prepared as a light yellow oil without further purification.
MS (ES) m/e 250 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.77 (q, 1H, J=8.0 Hz); 7.07 (m, 2H); 6.89 (dd, 1H, J1=8.1 Hz, J2=1.3 Hz); 6.77 (d, 1H, J=7.8 Hz); 6.65 (dd, 1H, J1=7.8 Hz, J2=2.1 Hz); 4.42 (s, 2H); 3.40 (s, 3H).
According to the procedure of example 20(a) except substituting 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 3,4-difluoronitrobenzene (318 mg; 2.0 mmol), the title compound (551 mg; 95%) was prepared as a yellow solid, used without further purification.
MS (ES) m/e 292 (M+H)+.
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 4-ethyl-1-(2-fluoro-4-nitrophenoxy)-2-methoxybenzene (551 mg; 1.89 mmol), two compounds were obtained after purification on silica gel (gradient: cyclohexane/ethyl acetate):
4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (202 mg; 40%)
MS (ES) m/e 262 (M+H)+.
4-{[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]amino}butan-1-ol (30 mg; 5%) MS (ES) m/e 334 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-{[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]amino}butan-1-ol (30 mg; 0.009 mmol), the title compound (24 mg; 83%) was prepared as a light brown solid, after purification by preparative TLC (dichloromethane/methanol: 95/5).
MS (ES) m/e 320 (M+H)+
1H RMN (CDCl3) δ (ppm): 6.90 (m, 2H); 6.60 (m, 2H); 6.42 (d, 1H, J=12.8 Hz); 6.33 (d, 1H, J=8.7 Hz); 3.71 (m, 2H); 3.12 (t, 2H, J=5.9 Hz); 2.56 (q, 2H, J=7.6 Hz); 1.70 (sl, 4H); 1.20 (t, 3H, J=7.6 Hz).
To a solution of 4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (215 mg; 0.82 mmol) in H2SO4 35%, at 0° C., was added a solution of NaNO2 (69 mg; 1 mmol) in water (1 mL). The mixture was stirred 30 min. at 0° C. A solution of copper(II) sulphate (1.85 g; 11.6 mmol) in 6 mL of water was added, followed by copper(I) oxide(99 mg; 0.69 mmol). The reaction was stirred 45 min. at room temperature, then hydrolysed with NaHCO3 sat(6 mL) and NH4OH. The mixture was extracted with ethyl acetate (3*5 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (85 mg; 0.032 mmol; 39%) was obtained as an oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 285 (M+Na)+
To a solution of 4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenol (0.32 mmol; 85 mg) in dry acetone (3 mL), under argon, were added potassium hydroxide (0.39 mmol; 54 mg), NaI (0.065 mmol; 10 mg) and N-(3-bromopropyl)phtalimide (0.40 mmol; 107 mg). The reaction was stirred 3 days at 50° C. The mixture was concentrated in vacuo, hydrolysed with NH4Cl sat.(5 mL) and extracted with ethyl acetate (3*3 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (75 mg; 0.17 mmol; 51%) was obtained as an oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 285 (M+Na)+
1H RMN (CDCl3) δ (ppm): 7.83 (dd, 2H, J1=5.2 Hz; J2=3.0 Hz); 7.71 (dd, 2H, J1=5.2 Hz; J2=2.9 Hz); 6.86 (t, 1H, J=9.1 Hz); 6.80 (s, 1H); 6.67 (s, 2H); 6.61 (dd, 1H, J1=12.1 Hz; J2=2.5 Hz); 6.50 (d, 1H, J=8.9 Hz); 3.98 (t, 2H, J=5.9 Hz); 3.91-3.87 (m, 5H); 2.61 (q, 2H, J=7.6 Hz); 2.20-2.16 (m, 2H); 1.23 (t, 3H, J=7.6 Hz).
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 2-{3-[4-(4-Ethyl-2-methoxy-phenoxy)-3-fluoro-phenoxy]-propyl}-isoindole-1,3-dione (64 mg; 0.14 mmol), the title compound was prepared in 83% yield (0.12 mmol; 52 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—30/70).
MS (ES) m/e 436 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.84 (dd, 2H, J1=5.4 Hz; J2=3.1 Hz); 7.71 (dd, 2H, J1=5.4 Hz; J2=3.0 Hz); 6.94 (t, 1H, J=9.0 Hz); 6.86 (s, 1H); 6.63-6.60 (m, 2H); 6.54-6.50 (m,1H); 3.98 (t, 2H, J=5.9 Hz); 3.90 (t, 2H, J=6.8 Hz); 2.56 (q, 2H, J=7.6 Hz); 2.17 (qt, 2H, J=6.2 Hz); 1.20 (t, 3H, J=7.6 Hz).
To a solution of 2-{3-[4-(4-Ethyl-2-hydroxy-phenoxy)-3-fluoro-phenoxy]-propyl}-isoindole-1,3-dione (0.096 mmol; 42 mg) in methanol (2 mL), under argon, was added hydrazine monohydrate (0.21 mmol; 10 μL). The reaction was heated to reflux for 1 h 30. After cooling to 0° C., the mixture was hydrolysed with HCl 1N and filtered. The filtrate was basified with NaOH 0.1 N (pH=11) and extracted with chloroform (3*5 ml). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (13 mg; 0.04 mmol; 44%) was obtained as yellow oil, after purification by preparative TLC (dichloromethane/methanol/NH4OH: 90/10/1).
MS (ES) m/e 306 (M+H)+
1H RMN (CDCl3) δ (ppm): 6.92 (t, 1H, J=9.1 Hz); 6.85 (s, 1H); 6.68 (dd, 1H, J1=12.1 Hz, J2=2.6 Hz); 6.63-6.56 (m,3H); 3.90 (t, 2H, J=6.8 Hz); 3.86 (sl, 2H); 2.96(sl, 2H); 2.56 (q, 2H, J=7.6 Hz); 1.97 (qt, 2H, J=6.2 Hz); 1.19 (t, 3H, J=7.6 Hz).
According to the procedure of example 30 except substituting O-methylhydroxylamine hydrochloride by (aminooxy)acetic acid hydrochloride (0.21 mmol; 23 mg), the title compound was isolated (43 mg; 65%) after purification by preparative (ethyl acetate/cyclohexane/acetic acid—40/60/1).
MS (ES) m/e 376 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.51 (dd, 1H, J1=12.0 Hz, J2=1.9 Hz); 7.32 (d, 1H, J=8.0 Hz); 6.96 (t, 1H, J=8.4 Hz); 6.89 (s, 1H); 6.75 (d, 1H, J=8.3 Hz); 6.66 (dd, 1H, J1=8.2 Hz, J2=1.6 Hz); 4.72 (s, 2H); 4.24 (q, 2H, J=7.1 Hz); 2.60 (q, 2H, J=7.6 Hz); 2.27 (s, 3H); 1.29 (t, 3H, J=7.1 Hz); 1.22 (t, 3H, J=7.6 Hz).
The title compound (11 mg; 18%) was isolated from the example 40 as a white solid, after purification by preparative TLC ethyl acetate/cyclohexane/acetic acid—40/60/1).
MS (ES) m/e 348 (M+H)+
1H RMN (MeOD) δ (ppm): 7.52 (d, 1H, J=12.5 Hz); 7.33 (d, 1H, J=8.3 Hz); 6.83-6.80 (m, 2H); 6.77 (t, 1H, J=8.0 Hz); 6.68 (dd, 1H, J1=8.2 Hz, J2=1.8 Hz); 4.86 (sl, 2H); 2.59 (q, 2H, J=7.6 Hz); 2.26 (s, 3H); 1.23 (t, 3H, J=7.6 Hz).
To a solution of 4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (0.38 mmol; 100 mg) in dry dichloromethane (1 mL), under argon, at 0° C. were added pyridine (0.46 mmol; 37 μL) and 3-chloropropanesulfonyle chloride (0.46 mmol; 56 μL). The reaction was stirred overnight at room temperature. The mixture was hydrolysed with NH4Cl sat.(2 mL) and extracted with dichloromethane (3*1 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (200 mg; 0.38 mmol; quantitative) was obtained as a brown oil, used without further purification.
MS (ES) m/e 306 (M+H)+
To a solution of 3-chloro-N-[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]propane-1-sulfonamide (0.38 mmol; 153 mg) in dry acetonitrile (2 mL), under argon, was added morpholine (1.1 mmol; 100 μL). The reaction was heated at 50° C. overnight. After cooling to room temperature, the mixture was hydrolysed with 5 mL of water and extracted with dichloromethane (3*2 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo, the title compound (62 mg; 36%) was obtained after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—40/60).
MS (ES) m/e 453 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.11 (dd, 1H, J1=12.0 Hz, J2=2.1 Hz); 6.84-6.72 (m, 5H); 3.83 (s, 3H); 3.69 (m, 4H); 3.19 (t, 2H, J=7.1 Hz); 2.64 (q, 2H, J=7.6 Hz); 2.51-2.47 (m, 6H); 2.04 (qt, 2H, J=6.8 Hz); 1.25 (t, 3H, J=7.6 Hz).
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 3-Morpholin-4-yl-propane-1-sulfonicacid[4-(4-ethyl-2-methoxy-phenoxy)-3-fluoro-phenyl]-amide (0.11 mmol; 50 mg), the title compound was prepared in 60% yield (0.07 mmol; 29 mg) after purification by preparative TLC (dichloromethane/methanol—95/5).
MS (ES) m/e 439 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.16 (dd, 1H, J1=11.7 Hz, J2=2.3 Hz); 6.95-6.88 (m, 3H); 6.73 (d, 1H, J=8.2 Hz); 6.65 (dd, 1H, J1=8.2 Hz, J2=1.9 Hz); 3.71 (t, 4H, J=4.2 Hz); 3.18 (t, 2H, J=7.0 Hz); 2.61-2.53(m, 8H); 2.06 (qt, 2H, J=6.8 Hz); 1.21 (t, 3H, J=7.6 Hz).
The title compound (44 mg; 31%) was isolated from the example 42(b) as a white solid, after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—40/60).
MS (ES) m/e 388 (M+Na)+
1H RMN (CDCl3) δ (ppm): 7.11 (dd, 1H, J1=12.0 Hz, J2=2.5 Hz); 6.94 (d, 1H, J=8.9 Hz); 6.87-6.80 (m,3H); 6.72 (dd, 1H, J1=8.1 Hz, J2=1.3 Hz); 3.83 (s, 3H); 3.71 (t, 2H, J=6.6 Hz); 3.38 (t, 2H, J=7.4 Hz); 2.63 (q, 2H, J=7.6 Hz); 2.51 (qt, 2H, J=7.6 Hz); 1.24 (t, 3H, J=7.6 Hz).
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 2-[4-(4-Ethyl-2-methoxy-phenoxy)-3-fluoro-phenyl]-isothiazolidine 1,1-dioxide (0.10 mmol; 38 mg), the title compound was prepared in 76% yield (0.08 mmol; 28 mg) after purification by preparative TLC on silica gel (dichloromethane/methanol—95/5).
MS (ES) m/e 374 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.11 (dd, 1H, J1=12.0 Hz, J2=2.5 Hz); 7.03-6.96 (m, 2H); 6.88 (sl, 1H); 6.70 (d, 1H, J=8.2 Hz); 6.63 (dd, 1H, J1=8.2 Hz, J2=1.8 Hz); 3.73 (t, 2H, J=6.6 Hz); 3.39 (t, 2H, J=7.4 Hz); 2.61-2.50 (m, 4H); 1.21 (t, 3H, J=7.6 Hz).
4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (0.19 mmol; 50 mg) in 1 mL THF/NaHCO3 sat. (1/1), at 0° C. were added ethylchloroformate (0.38 mmol; 41 mg). The reaction was stirred overnight at room temperature. The mixture was hydrolysed with NH4Cl sat.(4 mL) and extracted with dichloromethane (3*2 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (36 mg; 56%) was obtained as a brown oil, after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—70/30).
MS (ES) m/e 334 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by ethyl[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]carbamate (0.11 mmol; 35 mg), the title compound was prepared in 69% yield (0.07 mmol; 23 mg) after purification by preparative TLC (ethyl acetate/cyclohexane—70/30).
MS (ES) m/e 320 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.41 (d, 1H, J=12.0 Hz); 6.99-6.96 (m, 2H); 6.88 (sl, 1H); 6.67 (d, 1H, J=8.1 Hz); 6.62 (dd, 1H, J1=8.2 Hz, J2=1.8 Hz); 4.23 (q, 2H, J=7.1 Hz); 2.58 (q, 2H, J=7.6 Hz); 1.31 (t, 3H, J=7.1 Hz); 1.21 (t, 3H, J=7.6 Hz).
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 4-ethyl-1-(2-fluoro-4-nitrophenoxy)-2-methoxybenzene (1.16 g; 4.0 mmol) and tetrahydrofurane for ethanol (16 mL), two compounds were obtained after purification on silica gel (gradient cyclohexane/dichloromethane) 4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (466 mg; 45%)
MS (ES) m/e 262 (M+H)+
N-ethyl-4-(4-ethyl-2-methoxyphenox)-3-fluoroaniline (461 mg; 40%) MS (ES) m/e 290 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for N-ethyl-4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (461 mg; 1.59 mmol), the title compound (270 mg; 62%) was prepared as a light brown solid, after purification by chromatography on silica gel (gradient dichloromethane/ethyl acetate).
MS (ES) m/e 276 (M+H)+
1H RMN (CDCl3) δ (ppm): 6.93 (t, 1H, J=8.9 Hz); 6.87 (s, 1H); 6.62 (q, 2H, J=6.6 Hz); 6.46 (dd, 1H, J1=12.7 Hz, J2=2.5 Hz); 6.37 (d, 1H, J=8.7 Hz); 3.15 (q, 2H, J=7.2 Hz); 2.59 (q, 2H, J=7.6 Hz); 1.30 (t, 3H, J=7.1 Hz); 1.21 (t, 3H, J=7.6 Hz).
To acetic anhydride (0.53 mmol; 51 μL) under argon, at 0° C., was added formic acid (0.66 mmol; 25 μL). The reaction was stirred 2 hours at 60° C. After cooling to 0° C., the mixture was diluted with 1 mL of dry THF, followed by a solution of 2-(4-ethyl-2-methoxyphenoxy)aniline (0.21 mmol; 50 mg) in dry THE (1 mL). The reaction was stirred 2 hours at room temperature. The mixture was concentrated in vacuo to give the title compound (72 mg; quantitative) as a brown oil, used without further purification.
MS (ES) m/e 272 (M+H)+.
To a solution of N-[2-(4-ethyl-2-methoxyphenoxy)phenyl]formamide (0.21 mmol; 72 mg), under argon, in dry THF was added at 0° C., borane dimethylsulfide complex (0.51 mmol, 49 μL). The reaction was stirred at reflux for 3 h 30. After cooling to 0° C., the mixture was diluted with 1 mL of dry methanol and stirred 1 hour. HCl (4M in dioxane) was added at 0° C. until pH 2, then the mixture was refluxed 1 hour. After cooling to room temperature, the reaction was diluted with 5 mL of methanol and concentrated in vacuo. The crude was treated with 5 mL of NaOH (1N), until pH 12, and extracted with ethyl acetate (3*2mL). Combined organic phases were dried over Na2SO4 and concentrated in vacuo to yield the title compound (66 mg, quantitative) as a red oil used without further purification.
MS (ES) m/e 258 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 2-(4-ethyl-2-methoxyphenoxy)-N-methylaniline (0.26 mmol; 66 mg), the title compound was prepared in 50% yield (0.13 mmol; 31 mg) after purification by preparative TLC (ethyl acetate/cyclohexane—70/30).
MS (ES) m/e 244 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.07 (t, 1H, J=6.6 Hz); 6.88 (s, 1H); 6.81-6.76 (m, 3H); 6.69-6.64 (m, 2H); 2.89 (s, 3H); 2.60 (q, 2H, J=7.6 Hz); 1.23 (t, 3H, J=7.6 Hz).
To a suspension of Cu(OAc)2 (3.0 mmol; 543 mg), 4-(methanesulphonyl)benzeneboronic acid (4.0 mmol; 800 mg) and activated molecular sieves (800 mg) under air, in anhydrous dichloromethane (5 mL), were added 2-methoxy-4-ethylphenol (2.0 mmol; 0.28 mL), anhydrous triethylamine (10 mmol; 1.4 mL), and anhydrous pyridine (10 mmol; 0.8 mL). The reaction was stirred for 2 days at room temperature. The crude was filtered on silica gel, washed with ethyl acetate, concentrated. The residue was then purified by column chromatography (gradient cyclohexane/dichloromethane) to yield the title compound as clear oil (617 mg; 2.0 mmol; quantitative).
MS (ES) m/e 307 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-2-methoxyphenoxy)phenyl methyl sulfone (130 mg; 0.42 mmol), the title compound (94 mg; 76%) was prepared as a white solid, after purification by preparative TLC (dichloromethane).
MS (ES) m/e 293 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.91 (d, 2H, J=8.8 Hz); 7.13 (d, 2H, J=8.9 Hz); 6.95 (s, 1H) 6.92 (d, 1H, J=8.2 Hz); 6.78 (d, 1H, J=8.2 Hz); 3.07 (s, 3H); 2.66 (q, 2H, J=7.6 Hz); 1.26 (t, 3H, J=7.6 Hz).
According to the procedure of example 20(a) except substituting 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 3,4-difluoronitrobenzene (30.5 g; 192 mmol), and 2-methoxy-4-ethylphenol for 2-(benzyloxy)-4-ethylphenol (33.6 g; 147 mmol) the title compound (58.1 g; 100%) was prepared as a brown oil, used without further purification.
To a solution of 2-(benzyloxy)-4-ethyl-1-(2-fluoro-4-nitro phenoxy)benzene (25 g; 68 mmol) in ether (86 mL), under argon cooled to 0° C., was added a suspension of tin dichloride (153 g; 801 mmol) in HCl (50 mL; 2 mol). The mixture was allowed to warm up to room temperature overnight, then a 10% NaOH solution was added dropwise. The resulting mixture was extracted with ethyl acetate (5*400 mL). Combined organic phases were washed with water (400 mL) and brine, then dried over Na2SO4 and concentrated. The residue was purified on silica gel (ethyl acetate/cyclohexane 1:9) to yield the title compound as a light brown solid (15.8 g; 68.8%)
MS (ES) m/e 338 (M+H)+
4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluoroaniline (500 mg, 1.48 mmol), K2CO3 (1.23 g, 8.9 mmol) and 3-bromo-1-propanol (410 mg, 2.9 mmol) were taken in dry DMF (2 ml) in a microwave vial and was subjected to microwave at 180° C. for 2 h. The reaction mixture was filtered over celite and the residue washed thouroughly with ethyl acetate. The combined organic fractions including the filtrate were washed with water, brine, dried over Na2SO4 and concentrated. The crude obtained was combined with earlier crude products obtained from a 100 mg and 200 mg batches and purified together by column chromatography over silica gel using 40% ethylacetate in pet ether as eluant to get 400 mg (42.6%) of pure title compound.
3-[4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-phenylamino]-propan-1-ol (400 mg, 1.01 mmol) was taken in 15 ml of absolute ethanol, under nitrogen. To this was added Pd(OH)2, (20%, 50 mg) followed by ammonium formate (200 mg, 3.1 mmol). The reaction mixture was heated at 65° C. and monitored by TLC. After complete consumption of starting material (20 minutes), the heating was stopped and mixture cooled to rt. The reaction mixture was filtered through celite and the residue was washed with methanol. The combined filtrate was concentrated to obtain 300 mg of crude compound showing 70% by HPLC. The crude was purified by preparative HPLC (Column: C18 Symmetry (300×19 mm), 7μ, Mobile phase A: 20 mM ammonium acetate, Mobile phase B: Acetonitrile) to get 140 mg (45.3%) of title compound.
To a solution of 4-(4-ethyl-2-methoxyphenoxy)phenyl methyl sulfone (0.44 mmol; 136 mg), in anhydrous THF (1 mL), under argon, cooled to 0° C., was added sBuLi (1.2M in cyclohexane; 0.89 mmol; 0.74 mL). After stirring for 30 min, a solution of 1-BOC-2-Pyrrolidinone (0.44 mmol; 0.08 mL) in anhydrous THF (1 mL) was slowly added. The reaction was stirred at 0° C. for 30 min. then slowly warmed up to toom temperature overnight. The mixture was quenched with water and NH4Cl sat. (3 mL), extracted with ethyl acetate (2*3 mL), to yield a light yellow oil (164 mg), used without further purification.
MS (ES) m/e 374 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for (2E)-2-({[4-(4-ethyl-2-methoxyphenoxy)phenyl]sulfonyl}methylene)pyrrolidine (164 mg; 0.44 mmol), the title compound (34 mg; 0.09 mmol; 22%) was prepared as a clear oil, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 378 (M+H2O+H)+
1H RMN (CDCl3) δ (ppm): 7.78 (d, 2H, J=8.8 Hz); 6.99 (d, 2H, J=8.8 Hz); 6.90 (s, 1H); 6.87 (d, 1H, J=8.3 Hz); 6.73 (d, 1H, J=8.0 Hz); 4.66 (s, 1H); 3.75 (t, 2H, J=1.8 Hz); 2.79 (q, 2H, J=6.7 Hz); 2.63 (t, 2H, J=7.6 Hz); 1.95 (qu, 2H, J=7.1 Hz); 1.24 (t, 3H, J=7.6 Hz).
According to the procedure of example 20(a) except substituting 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 1,3-difluoro-4-nitrobenzene (110 μL; 1 mmol), the title products were obtained as a yellow solid (253 mg; 87%), after purification by preparative TLC (cyclohexane/ethyl acetate: 9/1).
MS (ES) m/e 292 (M+H)+.
To a solution of 4-ethyl-1-(3-fluoro-4-nitrophenoxy)-2-methoxybenzene and 4-ethyl-1-(5-fluoro-2-nitrophenoxy)-2-methoxybenzene (100.5 mg, 0.69 mmol) in ethanol (5 mL) was added Tin(II)chloride dihydrate (794 mg, 3.45 mmol). The reaction mixture was heated to reflux for 1 h 30. The reaction mixture was washed with water, solid sodium hydrogenocarbonate and a NaOH solution (1 N). The mixture was extracted with ethyl acetate. Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give the title products as a light brown oil (51 mg; 28%), after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 262 (M+H)+.
According to the procedure of example 5(b), except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for a mixture of 4-(4-ethyl-2-methoxyphenoxy)-2-fluoroaniline and 2-(4-ethyl-2-methoxyphenoxy)-4-fluoroaniline (50.9 mg, 0.19 mmol), the title compound (8.9 mg; 19%) was obtained after purification by preparative TLC (dichloromethane/ethyl acetate: 9/1).
MS (ES) m/e 248 (M+H)+
1H NMR (CDCl3) δ (ppm): 6.90-6.87 (m, 2H); 6.80-6.67 (m, 3H); 6.59 (dd, 1H, J1=2.8 Hz; J2=9.6 Hz); 2.62 (q, 2H, J=7.6 Hz); 1.25 (t, 3H, J=7.6 Hz).
According to the procedure of example 42(a) except substituting 3-chloropropanesulfonyle chloride by Trifluoroethanesulfonyl chloride (0.4 6 mmol; 84 mg), the title compound was prepared (177 mg; quantitative yield) as a brown oil used without further purification.
MS (ES) m/e 408 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by N-[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]-2,2,2-trifluoroethanesulfonamide (0.38 mmol; 156 mg), the title compound was prepared in 53% yield (0.20 mmol; 80 mg) after purification by preparative TLC (cyclohexane/ethyl acetate—7/3).
MS (ES) m/e 394 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.19 (dd, 1H, J1=11.4 Hz, J2=2.4 Hz); 7.11 (sl, 1H); 7.01-6.93 (m, 2H); 6.90 (d, 1H, J=1.9 Hz); 6.77 (d, 1H, J=8.2 Hz); 6.69 (dd, 1H, J1=8.2 Hz, J2=2.0 Hz); 3.83 (q, 2H, J=8.8 Hz); 2.60 (q, 2H, J=7.6 Hz); 1.24 (t, 3H, J=7.6 Hz).
According to the procedure of example 42(a) except substituting 3-chloropropanesulfonyle chloride by cyclopropanesulfonyl chloride (0.46 mmol; 47 μL), the title compound was prepared (170 mg; quantitative yield) as a brown oil used without further purification.
MS (ES) m/e 366 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by N-[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]cyclopropane sulfonamide (0.38 mmol; 140 mg), the title compound was prepared in 94% yield (0.36 mmol; 126 mg) after purification by preparative TLC (cyclohexane/ethyl acetate—7/3).
MS (ES) m/e 352 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.19 (d, 1H, J=11.8 Hz); 6.97 (m, 2H); 6.87 (m, 2H); 6.72 (d, 1H, J=8.3 Hz); 6.66 (dd, 1H, J1=8.3 Hz, J2=2.0 Hz); 2.59 (q, 2H, J=7.6 Hz); 2.51 (m, 1H); 1.24-1.17 (m, 5H); 1.03-0.98 (m; 2H)
According to the procedure of example 49(a) except substituting 1-BOC-2-Pyrrolidinone for propylene oxide (0.2 mL; 2.8 mmol), the title compound (200 mg; 0.56 mmol; 100%) was prepared as a yellow oil, used without purification.
MS (ES) m/e 365 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-{[4-(4-ethyl-2-methoxyphenoxy)phenyl]sulfonyl}butan-2-ol (200 mg; 0.56 mmol), the title compound (11 mg; 0.03 mmol; 6%) was prepared as a clear oil, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 351 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.81 (d, 2H, J=8.9 Hz); 7.08 (d, 2H, J=8.9 Hz); 6.90 (d, 2H, J=9.9 Hz); 6.75 (d, 1H, J=8.2 Hz); 5.6 (sl, 1H); 3.90 (m, 1H); 3.21 (m, 2H); 2.63 (q, 2H, J=7.6 Hz); 1.91 (m, 1H); 1.74 (m, 1H); 1.26 (t, 3H, J=7.6 Hz); 1.20 (d, 3H, J=6.2 Hz).
According to the procedure of example 20(a) except substituting 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 2-fluoro-4-nitrotoluene (157 mg; 1 mmol), the title compound (258 mg; 90%) was prepared as a yellow oil after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 288 (M+H)+.
According to the procedure of example 50(b) except substituting 4-(4-ethyl-2-methoxyphenoxy)-2-fluoroaniline and 2-(4-ethyl-2-methoxyphenoxy)-4-fluoroaniline for 4-ethyl-2-methoxy-1-[(5-methyl-2-nitro)phenoxy]benzene (257 mg, 0.90 mmol), the title compound was prepared as a brown oil (167 mg; 72%), after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 258 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-(4-ethyl-2-methoxyphenoxy)-4-methylaniline (66.4 mg, 0.26 mmol), the title compound was prepared as a brown solid (4.9 mg; 8%), after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 244 (M+H)+
1H NMR (CDCl3) δ (ppm): 6.89 (d, 1H, J=2 Hz); 6.83 (d, 1H, J=8 Hz); 6.79 (d, 1H, J=8 Hz); 6.75 (d, 1H, J=8 Hz); 6.68 (s, 1H); 6.66 (d, 1H, J=2 Hz); 2.61 (q, 2H, J=7.6 Hz); 2.21 (s, 3H); 1.24 (t, 3H, 1.24 Hz).
According to the procedure of example 21(a3) except substituting 4-ethyl-2-methoxyphenol by 2-methoxy-4-propylphenol (1.93 g, 11.61 mmol), the title compound was prepared in 86% yield (2.6 g) after purification on silica gel (eluant ethyl acetate/pet ether 15:85) as a pale yellow liquid.
1H NMR (CDCl3), δ (ppm): 8.16 (d, J=4.4 Hz, 1H), 7.42 (dd, J=8.4 Hz, J=4.4 Hz, 1H), 7.23 (d, J=8.4 Hz 1H), 7.05 (d, J=7.8 Hz, 1H), 6.8-6.83 (m, 2H ), 3.74 (s, 3H), 2.61 (t, J=7.4 Hz, 2H), 1.62-1.7 (m, 2H), 0.97 (t, J=7.4 Hz, 3H)
LC-MS m/z 289.1 (M+H)+
To a stirred solution of 3-(4-propyl-2-methoxyphenoxy)-2-nitropyridine (1.1 g, 3.8 mmol) in methanol (15 ml) was added anhydrous Ferric chloride (55 mg, 5% by wt) and activated charcoal (55 mg, 5% by wt). The resulting mixture was heated to reflux and hydrazine hydrate (570 mg, 11.45 mmol) was added dropwise. The reaction was allowed to stir under reflux condition overnight, then filtered through celite. The filtrate was concentrated under reduced pressure, taken in ethyl acetate (150 ml). The organic layer was washed with water followed by brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was passed through silica column (eluant ethylacetate/pet ether 1:3 to get 900 mg (91.3%) of title compound as a pale yellow solid.
1H NMR (CDCl3), δ (ppm): 7.74 (d, J=5.1 Hz, 1H), 6.9 (d, J=8 Hz, 1H), 6.8-6.83 (m, 2H), 6.76 (d, J=8.12 Hz, 1H), 6.56 (dd, J=7.8 Hz, J=5.2 Hz, 2H ), 5.09 (bs, 2H), 3.82 (s, 3H), 2.59 (t, J=7.4 Hz, 2H), 1.60-1.66 (m, 2H), 0.97 (t, J=7.3 Hz, 3H)
LC-MS m/z 259.1 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 3-(2-methoxy-4-propylphenoxy)pyridin-2-amine (0.9 g, 3.48 mmol), the title compound (0.52 g; 61%) was obtained.
1H NMR (DMSO-d6), δ (ppm): 9.4 (s, D2O exchangeable, 1H), 7.59 (d, J=4.9 Hz, 1H), 6.83 (d, J=8.08 Hz, 1H), 6.77 (d, J=1.6 Hz, 1H), 6.66-6.61 (m, 2H), 6.43 (dd, J=7.6 Hz, J=4.88 Hz, 1H), 5.82 (bs, D2O exchangeable, 2H), 2.46 (t, J=7.6 Hz, 2H), 1.58-1.52 (m, 2H), 0.88 (t, J=7.3 Hz, 3H)
LC-MS m/z 244.8 (M+H)+
To 2-(4-aminophenoxy)-5-ethyl-4-fluorophenol (785 mg, 3 mmol) were added toluene (1.5 mL) and succinic anhydride (360.3 mg, 3.6 mmol). The reaction was left to stir for 3 days at 110° C. under argon, then concentrated, dissolved in dichloromethane, washed with a saturted solution of NaHCO3 and a solution of KOH (1 M) and extracted with dichloromethane. Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give the title product as a white solid (624.3 mg; 61%), after purification on silica gel (dichloromethane).
MS (ES) m/e 344 (M+H)+
To 1-[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]pyrrolidine-2,5-dione (40.4 mg, 0.12 mmol) were added acetonitrile (120 μL) and morpholine (20 μL, 0.24 mmol). The reaction mixture was stirred at 30° C. for 3 days under argon, then concentrated, dissolved in ethyl acetate, washed with saturated NH4Cl and extracted with ethyl acetate. Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give the title product (45.1 mg; 87%) after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 431 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for N-[4-(4-Ethyl-2-methoxy-phenoxy)-3-fluoro-phenyl]-4-morpholin-4-yl-4-oxo-butyramide (45 mg, 0.10 mmol), the title compound was prepared as a white solid (29 mg; 69%), after purification by preparative TLC (dichloromethane/methanol: 95/5).
MS (ES) m/e 417 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.64 (dd, 1H, J1=2.4 Hz, J2=12.4 Hz); 7.10-7.07 (m, 1H); 6.97 (t, 1H, J=8.8 Hz); 6.89 (d, 1H, J=1.6 Hz); 6.68 (d, 1H, J=8.0 Hz); 6.63 (dd, 1H, J1=2 Hz, J2=8.4 Hz), 3.73-3.66 (m, 8 H), 2.76-2.73 (m, 4 H), 2.60 (q, 2H, J=1.6 Hz), 1.23 (t, 3H, J=1.6 Hz).
According to the procedure of example 20(a) except substituting 2-methoxy-4-propylphenol for 4-bromo-5-fluoro-2-methoxyphenol (441 mg; 2 mmol), and 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 2,6-Difluoropyridine (0.18 mL; 2 mmol), the title compound was prepared as a yellow oil (246 mg; 39%), after purification on silica gel (cyclohexane/ethyl acetate: 95/5).
MS (ES) m/e 317 (M+H)+.
To 2-(4-bromo-5-fluoro-2-methoxyphenoxy)-6-fluoropyridine (227 mg, 0.71 mmol) were added [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (58.9 mg, 0.07 mmol) and potassium carbonate (597 mg, 4.26 mmol). To the mixture were added acetonitrile (4 mL), water (1.3 mL) and vinyl boronic acid pinacol ester (180 μL, 1.07 mmol). The reaction was flushed with argon, and left to stir for 3 days at 60° C. The reaction mixture was then filtered on celite, rinsed with dichloromethane and concentrated. After purification by preparative TLC (cyclohexane/ethyl acetate: 70/30), the title product was isolated as an orange oil (166 mg, 89%).
MS (ES) m/e 264 (M+H)+.
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 2-fluoro-6-[(3-fluoro-4-vinyl-6-methoxy)phenoxy)]pyridine (166 mg; 0.63 mmol) and tetrahydrofurane for ethanol (2 mL), the title product was isolated (145.4 mg, 87%) after purification by preparative TLC (cyclohexane/ethyl acetate: 80/20).
MS (ES) m/e 266 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-fluoro-6-[(3-fluoro-4-ethyl-6-methoxy)phenoxy)]pyridine (145 mg, 0.55 mmol), the title compound (120.5 mg; 87%) was prepared as an oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 252 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.83 (q, 1H, J=8 Hz); 6.92 (d, 1H, J=7.6 Hz); 6.84 (d, 2H, J=9.6 Hz); 6.70 (dd, 1H, J=8 Hz); 2.65 (q, 2H, J=7.6 Hz); 1.26 (t, 3H, J=3.6 Hz).
According to the procedure of example 49(a) except substituting 1-BOC-2-Pyrrolidinone for 2-Bromomethyl-1,3-dioxolane (0.05 mL; 0.47 mmol), the title compound (152 mg; 0.39 mmol; 100%) was prepared as a yellow oil, used without purification.
MS (ES) m/e 393 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-{2-[4-(4-Ethyl-2-methoxy-phenoxy)-benzene sulfonyl]-ethyl}-[1,3]dioxolane (152 mg; 0.39 mmol), the title compound (3 mg; 0.02 mmol; 2%) was prepared as a clear oil, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 379 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.86 (d, 2H, J=8.8 Hz); 7.12 (d, 2H, J=8.8 Hz); 6.95 (d, 1H, J=1.7 Hz); 6.92 (d, 1H, J=8.2 Hz); 6.78 (d, 1H, J=8.2 Hz); 4.97 (t, 1H, J=3.9 Hz); 3.94 (m, 2H); 3.85 (m, 2H); 3.23 (m, 2H); 2.66 (q, 2H, J=7.6 Hz); 2.10 (m, 2H); 1.26 (t, 3H, J=7.6 Hz).
According to the procedure of example 44(a) except substituting 4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline for 4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluoroaniline (200 mg; 0.59 mmol) and ethylchloroformate by benzylchloroformate (150 μL; 0.73 mmol), the title compound (300 mg; quantitative) was prepared as a brown solid and used without further purification.
MS (ES) m/e 494 (M+Na)+
To a solution of [4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-phenyl]-carbamic acid benzyl ester (0.31 mmol; 145 mg), under argon, in dry THF cooled to −78° C., was added n-Butyl lithium 2.3M in THF (0.46 mmol; 200 μL). the reaction mixture was stirred ten minutes and (R)-glycidyl butyrate (0.34 mmol; 48 μL) was added. The reaction was stirred overnight with slow warming to room temperature. The mixture was treated with saturated NH4Cl and extracted with ethyl acetate. Combined organic phases were dried over Na2SO4 and concentrated in vacuo. The title compound (70 mg; 52%) was obtained as . . . after purification by preparative TLC (eluant: dichloromethane/methanol: 95/5).
MS (ES) m/e 438 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for (5R)-3-[4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one (0.16 mmol; 70 mg), the title compound (0.12 mmol; 41 mg; 73%) was obtained as a white solid after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 438 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.55 (dd, 1H, J1=12.6 Hz, J2=2.6 Hz); 7.10-7.07 (m, 1H); 6.98 (t, 1H, J=8.9 Hz); 6.88 (d, 1H, J=1.6 Hz); 6.68 (d, 1H, J=6.7 Hz); 6.63 (dd, 1H, J1=8.3 Hz, J2=1.7 Hz); 4.74 (m, 1H); 4.02-3.96 (m, 3H); 3.75 (dd, 1H, J1=12.7 Hz, J2=3.7 Hz); 2.58 (q, 2H, J=7.6 Hz); 1.21 (t, 3H, J=7.6 Hz).
According to the procedure of example 59(b) except substituting (R)-glycidyl butyrate for (R,S)-glycidyl butyrate (0.43 mmol; 60 μL), the title compound (240 mg; quantitative) was prepared and used without further purification.
MS (ES) m/e 438 (M+Na)+
To a solution of 3-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluoro phenyl]-5-hydroxymethyloxazolidin-2-one (240 mg, 0.54 mmol) in 5 ml of dry dichloromethane and 0.16 ml (1.1 mmol) of triethylamine, cooled to 0° C., was added a solution of methanesulfonyl chloride (0.06 ml, 0.76 mmol) in 0.5 ml of dichloromethane dropwise. The reaction was allowed to warm to rt overnight. The reaction mixture was diluted with 20 ml water, 20 ml of dichloromethane were added and the layers separated. The aqueous layer was extracted with dichloromethane and the combined dichloromethane fraction was dried over anhydrous Na2SO4 and concentrated. The crude residue obtained was column purified over silica gel using 20% ethyl acetate in petroleum ether as eluant to get 120 mg, 42.8% of the title compound.
LC-MS m/z 516.1 (M+H)+
To a solution of methanesulfonic acid 3-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl ester (120 mg, 0.23 mmol) in 2 ml of dry DMF under nitrogen was added sodium azide (57 mg, 0.88 mmol). The reaction mixture was stirred at 75° C. overnight. The reaction mixture was diluted with 15 ml water and extracted with ethyl acetate. The combined organic phase was washed with water, saturated brine solution, dried over anhydrous Na2SO4 and concentrated in vacuo to get 100 mg of the title compound which was used as such for the next step.
To a solution of 5-Azidomethyl-3-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluoro phenyl]-oxazolidin-2-one (100 mg, 0.16 mmol), in 15 ml of ethyl acetate, under nitrogen, was added palladium (10% Pd/C, 10 mg) and the mixture was stirred at rt under hydrogen overnight. The reaction mixture was filtered through celite and the residue was washed thoroughly with ethyl acetate. The combined filtrate was concentrated and the obtained crude compound was column purified over silica gel using a mixture of 5% methanol in chloroform as eluant to obtain 70 mg 74.4% of the reduced product 5-Aminomethyl-3-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]-oxazolidin-2-one. Debenzylation of this 70 mg was achieved by repeating the reaction using methanol as solvent, to obtain 30 mg, 54.1% of the title compound.
1H NMR (CD3OD), δ (ppm): 7.64 (dd, J=13.12, J=2.6 Hz, 1H), 7.17-7.14 (m, 1H), 6.87 (t, J=9 Hz, 1H), 6.8 (d, J=1.96 Hz, 1H), 6.74 ( d, J=8.16 Hz, 1H), 6.64 (dd, J=8.16 Hz, J=1.88 Hz, 1H), 4.74-4.70 (m, 1H), 4.12 (t, J=8.96 Hz, 1H), 3.82 (dd, J=8.96 Hz, J=6.8 Hz, 1H), 2.99-2.92 (m, 2H), 2.57 (q, J=7.6 Hz, 2H), 1.22 (t, J=7.6 Hz, 3H)
LC-MS m/z 347.1 (M+H)+
To a solution of 5-Aminomethyl-3-[4-(4-ethyl-2-hydroxyphenoxy)-3-fluorophenyl]-oxazolidin-2-one (10 mg, 0.028 mmol) in 2 ml of dry dichloromethane, cooled to 0° C., was added acetic anhydride (3 mg, 0.028 mmol) taken in 0.2 ml of dichloromethane. The reaction mixture was warmed to rt and stirred for 5 minutes until reaction was complete on TLC. The reaction mixture was diluted with 3 ml of water and the layers separated. The aqueous layer was extracted with dichloromethane and the combined organic fraction was dried over anhydrous Na2SO4 and concentrated. The crude residue obtained was purified by preparative HPLC (Column: C18 Symmetry (300×19 mm), 7μ, Mobile phase A: 20 mM ammonium acetate, Mobile phase B: Acetonitrile) to get 6 mg, 55.2% of the title compound.
1H NMR (CDCl3), δ (ppm): 7.58 (d, J=12.4, 1H), 7.09-7.02 (m, 2H), 6.9 (s, 1H), 6.71-6.64 (m, 2H), 6.15 (bs, 1H), 4.79 (bs, 1H), 4.04 (t, J=8.1 Hz, 1H), 3.80-3.62 (m, 3H), 2.57 (q, J=7.6 Hz, 2H), 2.25 (s, 3H), 1.22 (t, J=7.6 Hz, 3H)
LC-MS m/z 389.2 (M+H)+
According to the procedure of example 20(a) except substituting 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 4-fluoronitrobenzene (210 μL; 2 mmol) and 2-methoxy-4-ethylphenol for 4-bromo-5-fluoro-2-methoxyphenol (444 mg; 2 mmol), the title compound (527 mg; 77%) was prepared as a light yellow solid after purification on silica gel (cyclohexane/ethyl acetate: 95/5).
According to the procedure of example 57(b) except substituting 2-(4-bromo-5-fluoro-2-methoxyphenoxy)-6-fluoro pyridine for 4-[(3-fluoro-4-bromo-6-methoxy)phenoxy)]nitrobenzene (200.3 mg, 0.58 mmol), the title product was isolated as an orange oil (129.7 mg, 77%) after purification by preparative TLC (cyclohexane/ethyl acetate: 70/30).
MS (ES) m/e 290 (M+H)+.
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 4-[(3-fluoro-4-vinyl-6-methoxy) phenoxy)]nitrobenzene (129 mg; 0.44 mmol) and tetrahydrofurane for ethanol (3 mL), the title compound was isolated as an oil (45 mg, 39%) after purification by preparative TLC (cyclohexane/ethyl acetate: 70/30).
MS (ES) m/e 262 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-5-fluoro-2-methoxyphenoxy)aniline (44 mg, 0.17 mmol), the title compound (7.9 mg; 19%) was prepared as a brown powder, after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 248 (M+H)+
1H NMR (CDCl3) δ (ppm): 6.89 (d, 2H, J=8.8 Hz); 6.84 (d, 1H, J=7.2 Hz); 6.70 (d, 2H, J=9.2 Hz); 6.55 (d, 1H, J=10.4 Hz); 2.60 (q, 2H, J=7.6 Hz); 1.21 (t, 3H, J=7.6 Hz).
According to the procedure of example 21(a3) except substituting 4-Ethyl-2-methoxy phenol by 4-bromoguaïacol (2.51 mmol; 510 mg) and 3-Fluoro-2-nitropyridine by 3,4-difluoronitrobenzene (2.76 mmol; 305 μL), the title compound was prepared as a clear oil in quantitative yield (855 mg) and used without further purification.
According to the procedure of example 50(b) except substituting 4-ethyl-1-(3-fluoro-4-nitrophenoxy)-2-methoxybenzene and 4-ethyl-1-(5-fluoro-2-nitrophenoxy)-2-methoxy benzene for 4-bromo-1-(2-fluoro-4-nitrophenoxy)-2-methoxy benzene (1.88 mmol; 644 mg), the title compound (87%, 512 mg) was obtained as a red oil, and used without further purification.
MS (ES) m/e 312, 314 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-bromo-2-methoxyphenoxy)-3-fluoroaniline (1.64 mmol; 512 mg), the desired compound was prepared as a dark solid in 72% yield (350 mg) and used without further purification.
MS (ES) m/e 297, 299 (M+H+)
To a solution of 2-(4-amino-2-fluorophenoxy)-5-bromophenol (0.62 mmol; 185 mg) in dry dichloromethane (3 mL), under argon, were added to 0° C. diisopropylethylamine (2.01 mmol; 350 μL) and (Boc)2O (2.01 mmol, 439 mg). The reaction was stirred with a gradual warming to room temperature. The mixture was treated with saturated NH4Cl and extracted with dichloromethane. Combined organic layers were dried over Na2SO4 and concentrated in vacuo to give a brown oil (quantitative, 363 mg) used without further purification.
MS (ES) m/e 620, 622 (M+Na+)
According to the procedure of example 11(a) except substituting 5-bromo-2-(2-methoxy-4-propylphenoxy)pyridine by O,N,N-triBoc-2-(4-amino-2-fluorophenoxy)-5-bromophenol (0.62 mmol; 363 mg) and 3-butyn-1-ol by 3-ethynylthiophene (1.55 mmol; 153 μL), the title compound was obtained as a yellow solid (60%, 195 mg) after purification on silica gel (cyclohexane/ethyl acetate gradient).
MS (ES) m/e 548 (M+Na)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for O,N,N-triBoc-2-(4-amino-2-fluorophenoxy)-5-bromophenol (0.37 mmol; 195 mg) and THF by ethanol, a mixture of title compounds (167 mg; ≈80%) was obtained as a yellow oil, used without further purification.
MS (ES) m/e 550, 552 (M+H)+
To a mixture of O,N-diBoc-2-(4-amino-2-fluorophenoxy)-5-[2-(3-thienyl)ethyl]phenol and O,N-diBoc-2-(4-amino-2-fluorophenoxy)-5-[(E)-2-(3-thienyl)vinyl]phenol (0.31 mmol; 162 mg) in dry THF (2 mL), cooled to 0° C. under argon, was added TFA (13 mmol, 1 mL). The reaction was stirred overnight with gradual warming to rt. The mixture was treated with saturated NaHCO3 and extracted with ethyl acetate. Combined organic layers were dried and concentrated in vacuo, the title mixture was obtained (44 mg, ≈43%) as a white solid after purification on preparative TLC.
MS (ES) m/e 328, 330 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene by a mixture of 2-(4-amino-2-fluorophenoxy)-5-[2-(3-thienyl)ethyl]phenol and 2-(4-amino-2-fluorophenoxy)-5-[(E)-2-(3-thienyl)vinyl]phenol (0.13 mmol; 44 mg), and THF by ethanol, the title compound was prepared in 14% yield (0.02 mmol; 6 mg) as a brown oil after purification by preparative TLC (cyclohexane/ethyl acetate—7/3).
MS (ES) m/e 330 (M+H)+
1H RMN (MeOD) δ (ppm): 7.27 (dd, 1H, J1=4.9 Hz, J2=3.0 Hz); 6.98 (m, 1H); 6.93 (dd, 1H, J1=4.9 Hz, J2=1.2 Hz); 6.79 (t, 1H, J=8.9 Hz); 6.73 (d, 1H, J=1.3 Hz); 6.57-6.52 (m, 3H); 6.46 (ddd, 1H, J1=8.6 Hz, J2=2.6 Hz, J3=1.2 Hz); 2.91-2.87 (m, 2H); 2.82-2.78 (m, 2H).
According to the procedure of example 20(a) except substituting 1-fluoro-4-nitro-2-(trifluoromethyl)benzene for 1,2-difluoro-4-(methylsulphonyl)benzene (310 mg; 1.6 mmol), the title compound (581 mg; 100%) was prepared as a light brown solid, used without further purification.
MS (ES) m/e 325 (M+H)+.
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl methyl sulfone (63 mg; 0.19 mmol), the title compound (38 mg; 0.12%) was prepared as a clear oil, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 311 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.73 (dd, 1H, J1=9.7 Hz, J2=2.1 Hz); 7.61 (d, 1H, J=8.6 Hz); 7.03 (t, 1H, J=8.5 Hz); 6.94 (s, 1H); 6.89 (d, 1H, J=8.2 Hz); 6.77 (dd, 1H, J1=8.2 Hz; J2=2.0 Hz); 5.65 (sl, 1H); 3.07 (s, 3H); 2.64 (q, 2H, J=7.6 Hz); 1.25 (t, 3H, J=7.6 Hz).
NaNO2 (1.5 mmol; 103 mg) was slowly added to a solution of 4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (1.0 mmol; 261 mg) in acetonitrile (8 mL), AcOH (0.8 mL), and conc. HCl (0.5 mL), under argon at 0° C., in the dark. After 30 min. stirring, this solution was slowly added to a solution of H2SO3 (50 mmol; 4 mL), and NaCl (10 mmol; 580 mg) cooled to 0° C. CuCl2 (2 mmol; 268 mg) was slowly added. The reaction was stirred with slow warming to room temperature for 3 hr, then heated to 50° C. for 30 min. Cooled to 0° C., the mixture was slowly hydrolysed with conc NH3, extracted with dichloromethane (3*5 mL). Combined organic phases were dried over Na2SO4, concentrated, to yield a brown oil (344 mg; 1.0 mmol; quantitative), used as such in the following reactions.
MS (ES) m/e 341 (M−Cl+MeOH)
Conc. NH3 (5.0 mmol; 0.28 mL) was slowly added to a solution of 4-(4-ethyl-2-methoxyphenoxy)-3-fluorobenzenesulfonyl chloride (1.0 mmol; 344 mg) in THF (5 mL), under argon at 0° C. The reaction was stirred overnight with slow warming to room temperature. Diluted with ethyl acetate (5 mL), the mixture was washed with HCl (1N), and sat. NH4Cl. The organic phase was dried over MgSO4, concentrated. The residue was purified by chromatography (dichloromethane/ethyl acetate gradient) to yield the title compound as an off-white solid (108 mg; 0.33 mmol; 33%).
MS (ES) m/e 326 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-2-hydroxyphenoxy)-3-fluorobenzene sulfonamide (108 mg; 0.33 mmol), the title compound (18 mg; 0.06 mmol; 18%) was obtained as a white solid, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 311 (M+H)+
1H RMN (MeOD) δ (ppm): 7.76 (dd, 1H, J1=10.5 Hz, J2=2.0 Hz); 7.61 (d, 1H, J=8.6 Hz); 6.96 (d, 1H, J=8.2 Hz); 6.90-6.86 (m, 2H); 6.77 (d, 1H, J=8.2 Hz); 2.66 (q, 2H, J=7.6 Hz); 1.29 (t, 3H, J=7.6 Hz).
To 4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline (261.2 mg, 1 mmol) were added methanol (4 mL) and nicotinaldehyde (120 μL, 1.2 mmol). The reaction was stirred at 30° C. for 17 h under argon. To the reaction mixture was added NaBH4 (38 mg, 1 mmol). The reaction was stirred at 30° C. for 4 h under argon. The resulting mixture was concentrated in vacuo, dissolved in dichloromethane, washed with a saturated solution of NH4Cl and extracted with dichloromethane. Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give the title product as a yellow oil (160.5 mg; 46%), after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 353 (M+H)+
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 4-(4-ethyl-2-methoxyphenoxy)-3-fluoro-N-(pyridin-3-ylmethyl)aniline (63.5 mg, 0.18 mmol), the title product as a brown solid (9.5 mg; 12%), after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 339 (M+H)+
1H NMR (CDCl3) δ (ppm): 8.65 (s, 1H); 8.57 (d, 1H, J=4 Hz); 7.53 (d, 1H, J=8 Hz); 7.32 (m, 1H); 6.95 (t, 1H, J=8 Hz); 6.87 (s, 1H); 6.62 (m, 2H); 6.45 (dd; 1H; J1=12.4 Hz, J2=2.8 Hz); 6.37 (dd, 1H, J1=12 Hz, J2=4 Hz); 4.36 (s, 2H); 2.58 (q, 2H, 7.6 Hz); 1.22 (t, 3H, J=7.6 Hz).
According to the procedure of example 65(b) except substituting NH3 for 2-Methoxyethylamine (0.33 mL; 3.8 mmol), the title compound (118 mg; 0.30 mmol; 32%) was obtained as a yellow oil, after purification by chromatography (cyclohexane/dichloromethane gradient).
MS (ES) m/e 384 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-2-methoxyphenoxy)-3-fluoro-N-(2-methoxy ethyl)benzenesulfonamide (116 mg; 0.30 mmol), the title compound (45 mg; 0.13 mmol; 42%) was obtained as a clear oil, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 356 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.63 (dd, 1H, J1=10.0 Hz, J2=2.0 Hz); 7.50 (d, 1H, J=8.7 Hz); 6.94-6.87 (m, 3H); 6.73 (d, 1H, J=8.3 Hz); 5.64 (t, 1H, J=5.8 Hz); 3.64 (t, 2H, J=4.7 Hz); 3.05 (q, 2H, J=4.8 Hz); 2.61 (q, 2H, J=7.6 Hz); 1.24 (t, 3H, J=7.6 Hz).
According to the procedure of example 66(a) except substituting nicotinaldehyde for 1H-imidazole-2-carboxaldehyde (119 mg, 1.2 mmol), the title compound was prepared as a light yellow solid (288.2 mg; 85%), after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 342 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-2-methoxyphenoxy)-3-fluoro-N-(1H-imidazol-2-ylmethyl)aniline (288 mg, 0.84 mmol), the title compound was prepared as a brown oil (72.3 mg; 26%), after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 328 (M+H)+
1H NMR (MeOD) δ (ppm): 7.04 (s, 2H); 6.87 (t, 1H, J=8.8 Hz); 6.79 (d, 1H, J=1.2 Hz); 6.61-6.51 (m, 3H); 6.44 (dd, 1H, J1=8.8 Hz, J2=2.0 Hz); 4.41 (s, 2H); 2.58 (q, 2H, 7.6 Hz); 1.24 (t, 3H, 7.6 Hz).
To a solution of 4-(4-ethyl-2-hydroxyphenoxy)-3-fluorobenzenesulfonamide (0.28 mmol; 90 mg) in anhydrous dichloromethane (1 mL), under argon were added EDAC (0.36 mmol; 69 mg), DMAP (0.31 mmol; 38 mg) and acetic acid (0.36 mmol; 0.02 mL). The reaction was stirred overnight at room temperature. Diluted with dichloromethane (3 mL), the mixture was washed with HCl (1N; 3 mL). The organic phase was dried over MgSO4, concentrated to yield the desired compound as a yellow foam (90 mg; 0.25 mmol; 89%), used as such in the following reaction.
MS (ES) m/e 368 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for N-{[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]sulfonyl}acetamide (90 mg; 0.25 mmol), the title compound (46 mg; 0.13 mmol; 52%) was obtained as a clear oil, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 354 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.81 (dd, 1H, J1=9.9 Hz, J2=2.0 Hz); 7.70 (d, 1H, J=8.7 Hz); 6.96-6.86 (m, 3H); 6.75 (d, 1H, J=8.2 Hz); 2.62 (q, 2H, J=7.6 Hz); 2.06 (s, 3H); 1.25 (t, 3H, J=7.6 Hz).
N-Acetylethylenediamine (1.1 mmol; 0.10 mL) was slowly added to a solution of 4-(4-ethyl-2-methoxyphenoxy)-3-fluorobenzenesulfonyl chloride (0.94 mmol; 325 mg) and TEA (2.8 mmol; 0.40 mL) in anhydrous THF (5 mL), under argon at 0° C. The reaction was stirred overnight with progressive warming to room temperature. Concentrated, the mixture was purified by chromatography (dichloromethane/methanol/ammonia gradient) to yield the title compound as a yellow oil (142 mg; 0.35 mmol; 37%) used as such in the following reaction.
MS (ES) m/e 411 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for N-{2-[4-(4-Ethyl-2-methoxy-phenoxy)-3-fluoro-benzene sulfonylamino]-ethyl}-acetamide (142 mg; 0.35 mmol), the title compound (44 mg; 0.11 mmol; 32%) was obtained as a clear oil, after purification by preparative TLC (dichloromethane/methanol).
MS (ES) m/e 397 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.58 (dd, 1H, J1=10.0 Hz, J2=2.0 Hz); 7.44 (d, 1H, J=8.7 Hz); 6.91-6.88 (m, 2H); 6.84 (t, 1H, J=8.2 Hz); 6.74-6.68 (m, 2H); 6.10 (br, 1H); 3.23 (br, 2H); 2.98 (br, 2H); 2.59 (q, 2H, J=7.6 Hz); 1.88 (s, 3H); 1.24 (t, 3H, J=7.6 Hz).
According to the procedure of example 65(a) except substituting 4-(4-ethyl-2-methoxyphenoxy)-3-fluoroaniline for 4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluoroaniline (1.3 g; 3.8 mmol), the title compound (1.51 g; 3.6 mmol; 95%) was obtained as a brown oil used without purification in the following reaction.
MS (ES) m/e 417 (M−Cl+MeOH)+
According to the procedure of example 65(b) except substituting 4-(4-ethyl-2-methoxyphenoxy)-3-fluorobenzene sulfonyl chloride for 4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluorobenzene sulfonyl chloride and NH3 for propylamine (1.7 mmol; 0.14 mL), the title compound (140 mg; 0.32 mmol; 41%) was obtained as a brown oil after purification on preparative TLC (dichloromethane).
MS (ES) m/e 444 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-N-propyl-benzenesulfonamide (140 mg; 0.32 mmol) and tetrahydrofurane for ethanol (3 mL), the title compound (70 mg; 62%) was obtained as a clear oil, after purification on preparative TLC (dichloromethane)
MS (ES) m/e 354 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.65 (dd, 1H, J1=10.0 Hz, J2=2.1 Hz); 7.54 (d, 1H, J=9.5 Hz); 6.95 (t, 1H, J=8.5 Hz); 6.93 (d, 1H, J=1.9 Hz); 6.87 (d, 1H, J=8.2 Hz); 6.75 (d, 1H, J=8.2 Hz); 5.84 (br, 1H); 4.92 (t, 2H, J=6.1 Hz); 2.92 (q, 2H, J=6.5 Hz); 2.63 (q, 2H, J=7.6 Hz); 1.51 (se, 2H, J=7.2 Hz); 1.24 (t, 3H, J=7.6 Hz); 0.88 (t, 3H, J=7.5 Hz).
To 1-[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]pyrrolidine-2,5-dione (169.8 mg, 0.49 mmol) was added methanol (2 mL). The reaction mixture was stirred for 1 h 30 at room temperature under argon. Acetonitrile (2 mL) and NaBH4 (190.7 mg, 4.9 mmol) were added to the reaction. The reaction mixture was stirred at 50° C. for 17 h. Then it was concentrated, dissolved in dichloromethane, washed with a saturated solution of NH4Cl and extracted with dichloromethane. Combined organic phases were dried over Na2SO4, concentrated in vacuo, to give the title product as a white solid used without further purification (169.5 mg; 100%).
MS (ES) m/e 348 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for N-[4-(4-ethyl-2-methoxyphenoxy)-3-fluorophenyl]-4-hydroxybutanamide (47.9 mg, 0.14 mmol), the title compound was prepared as a colorless oil (16.5 mg; 35%), after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 334 (M+H)+
1H NMR (CD3OD) δ (ppm): 7.68 (dd, 1H, J1=12.8 Hz, J2=2.4 Hz); 7.19 (m, 1H); 6.88 (m, 2H); 6.76 (d, 1H, J=8.0 Hz); 6.68 (dd, 1H, J1=8.4 Hz, J2=2.0 Hz); 3.68 (t, 2H, J=6.2 Hz); 2.62 (q, 2H, J=7.6 Hz), 2.51 (t, 2H, J=7.6 Hz), 1.96 (qt, 2H, J=6.8 Hz); 1.27 (t, 3H, 7.6 Hz).
According to the procedure of example 21(a3) except substituting 4-Ethyl-2-methoxy phenol by 2-(benzyloxy)-4-ethylphenol (1.3 g, 5.7 mmol) and 3-Fluoro-2-nitropyridine by 1-(3,4-difluorophenyl)ethanone (0.98 g, 6.27 mmol), the title compound was prepared as a clear oil in 96% yield (2 g) and used without further purification.
LCMS m/z 365.0 (M+H)+
To a solution of 1-{4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluorophenyl}ethanone (3 g, 8.24 mmol) in dry dichloromethane (30 ml), was added PTSA (0.047 g,0.247 mmol). The reaction mixture was cooled in an ice bath and mCPBA (50% H2O) (2.84 g, 8.24 mmol) was added portionwise. The resulting mixture was stirred at RT for 3 days, then concentrated at 35-40 C. The residue was purified by column chromatography, (pet ether:EtOAC). The resulting solid was dissolved in pet ether, filtered then concentrated the yield the title compound (1.6 g; 51%)
LCMS m/z 379.2 (M−H)−
To a solution of 4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluorophenyl acetate (1.6 g, 4.2 mmol) in MeOH:H2O (35 ml:35 ml), was added KOH (0.83 g, 14.8 mmol). The mixture was heated at 65° C. for 4.5 hours, concentrated in vacuo, then extracted with EtOAC (25 ml*2). Combined organic phases were dried over Na2SO4 and concentrated. The residue was purified by column chromatography, (pet ether: EtOAC 95:5), to yield the title compound as a white solid (630 mg; 44%)
LCMS m/z 336.9 (M−H)−
To a solution of 4-[2-(benzyloxy)-4-ethylphenoxy]-3-fluorophenol (0.30 mmol; 100 mg) in dry acetone (2 mL), under argon, were added potassium carbonate (0.35 mmol; 49 mg), NaI (0.06 mmol; 9 mg) and ethyl bromobutyrate (0.35 mmol; 51 μL). The reaction was stirred 14 hours at 60° C. Water (100 μL) and tetrabutylammonium hydroxyde (0.03 mmol; 8 mg) were added and the mixture was stirred 16 hours at 60° C. The reaction was hydrolysed with NH4Cl sat. (5 mL) and extracted with ethyl acetate (3*3 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (100 mg; 0.22 mmol; 75%) was obtained as a yellow oil, after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 475 (M+Na)+
According to the procedure of example 48(d) except substituting 3-[4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-phenylamino]-propan-1-ol for 4-[4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-phenoxy]-butyric acid ethyl ester (0.22 mmol; 100 mg) the title compound was prepared as a clear oil (58 mg; 72%), after purification by preparative TLC (Cyclohexane/Ethyl acetate: 7/3)
MS (ES) m/e 363 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.00 (t, 1H, J=9.1 Hz); 6.87 (s, 1H); 6.74 (dd, 1H, J1=12.1 Hz, J2=2.8 Hz); 6.64-6.59 (m, 3H); 4.15 (q, 2H, J=7.1 Hz); 3.98 (t, 2H, J=6.1 Hz); 2.57 (q, 2H, J=7.6 Hz); 2.51 (t, 2H, J=7.3 Hz); 2.11 (qt, 2H, J=7.0 Hz); 1.27 (t, 3H, J=7.1 Hz); 1.21 (t, 3H, J=7.6 Hz).
To a solution of ethyl ethyl 4-[4-(4-Ethyl-2-hydroxy-phenoxy)-3-fluoro-phenoxy]-butyric acid ethyl ester (0.16 mmol; 58 mg), in a THF/water mixture (1/1; 1 mL) was added lithium hydroxide (0.64 mmol; 15 mg). The reaction was heated 1 hour at 60° C. After cooling to 0° C., the reaction was treated with concentrated HCl, and extracted with ethyl acetate (3*2 mL). Combinated organic phases were dried over Na2SO4 and concentrated in vacuo. The title compound (0.16 mmol; 54 mg; quantitative) was obtained as a clear oil, used without purification.
MS (ES) m/e 335 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.00 (t, 1H, J=9.7 Hz); 6.87 (s, 1H); 6.74 (dd, 1H, J1=12.1 Hz, J2=2.8 Hz); 6.64-6.59 (m, 3H); 3.99 (t, 2H, J=6.0 Hz); 2.61-2.55 (m, 4H); 2.13 (qt, 2H, J=6.9 Hz); 1.23 (t, 3H, J=7.6 Hz).
According to the procedure of example 70(a) except substituting N-Acetylethylenediamine for 2-(2-Aminoethyl) pyridine (1.5 mmol; 0.18 mL), the title compound (150 mg; 0.30 mmol; 24%) was obtained as a yellow oil after purification via chromatography. (gradient dichloromethane/ethyl acetate).
MS (ES) m/e 507 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-N-(2-pyridin-2-yl-ethyl)-benzene sulfonamide (150 mg; 0.30 mmol) and tetrahydrofurane for ethanol (3 mL), the title compound (70 mg; 62%) was obtained as a clear oil, after purification via preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 417 (M+H)+
1H RMN (CDCl3) δ (ppm): 8.41 (d, 1H, J=4.8 Hz); 7.62 (t, 1H, J=9.4 Hz); 7.53 (d, 1H, J=10.0 Hz); 7.45 (d, 1H, J=8.7 Hz); 7.17-7.13 (m, 2H); 6.91-6.85 (m, 3H); 6.73 (d, 1H, J=8.2 Hz); 6.14 (br, 1H); 3.32 (t, 2H, J=5.8 Hz); 2.94 (t, 2H, J=6.3 Hz); 2.62 (q, 2H, J=7.6 Hz); 1.23 (t, 3H, J=7.6 Hz)
According to the procedure of example 70(a) except substituting N-Acetylethylenediamine for 1-(3-Aminopropyl)imidazole (1.5 mmol; 0.18 mL), the title compound (160 mg; 0.31 mmol; 25%) was obtained as a brown oil after purification by preparative TLC (dichloromethane/methanol).
MS (ES) m/e 510 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 4-(2-Benzyloxy-4-ethyl-phenoxy)-3-fluoro-N-(3-imidazol-1-yl-propyl)-benzenesulfonamide (160 mg; 0.31 mmol) and tetrahydrofurane for ethanol (3 mL), the title compound (55 mg; 42%) was obtained as a clear oil, after purification via preparative TLC (dichloromethane/methanol/triethylamine)
MS (ES) m/e 420 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.52 (d, 1H, J1=10.0 Hz); 7.43 (d, 1H, J=8.7 Hz); 7.23 (s, 1H); 6.96-6.92 (m, 3H); 6.83-6.80 (m, 2H); 6.72 (d, 1H, J=8.2 Hz); 3.97 (t, 2H, J=6.4 Hz); 2.81 (t, 2H, J=6.3 Hz); 2.61 (q, 2H, J=7.6 Hz); 1.94 (q, 2H, J=6.3 Hz); 1.23 (t, 3H, J=7.6 Hz)
According to the procedure of example 66(a) except substituting nicotinaldehyde for 4(5)-imidazole carboxadehyde (115.27 mg, 1.2 mmol), the title compound was prepared as a colorless oil (300 mg; 88%), after purification by preparative TLC (dichloromethane/methanol: 95/5+1% NH4+).
MS (ES) m/e 342 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4(4-ethyl-2-methoxyphenoxy)-3-fluoro-N-(1H-imidazol-4-ylmethyl)aniline (300 mg, 0.87 mmol), the title compound (101 mg, 35%) was prepared as a white solid, after purification by preparative TLC and washing with diethyl ether (dichloromethane/methanol: 95/5+1% NH4+).
MS (ES) m/e 328 (M+H)+
1H NMR (MeOD) δ (ppm): 7.62 (s, 1H), 6.97 (s, 1H), 6.79 (t, 1H, J=9.0 Hz), 6.71 (s, 1H), 6.51-6.50 (m, 3H), 6.42 (dd, 1H, J1=8.8 Hz, J2=3.8 Hz), 4.20 (s, 2H), 2.51 (q, 2H, J=7.6 Hz), 1.16 (t, 3H, J=7.6 Hz)
According to the procedure of example 11(a) except substituting 5-bromo-2-(2-methoxy-4-propylphenoxy)pyridine by 2-(4-bromo-2-methoxyphenoxy)-6-fluoropyridine (0.98 mmol; 300 mg) and 3-butyn-1-ol by propargylic alcohol (2.50 mmol; 150 μL), the title compound was obtained as a yellow solid (71%, 191 mg) after purification on silica gel (cyclohexane/ethyl acetate gradient).
MS (ES) m/e 274 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene by 3-{4-[(6-fluoropyridin-2-yl)oxy]-3-methoxyphenyl}prop-2-yn-1-ol (0.33 mmol; 90 mg) and THF by absolute ethanol, the title compound (quantitative, 102 mg) was obtained as a yellow oil, and used without further purification.
MS (ES) m/e 339 (M+H)+
To a solution of 3-{4-[(6-fluoropyridin-2-yl)oxy]-3-methoxyphenyl}prop-2-yn-ol (0.37 mmol; 102 mg) in dry dichloromethane (2 mL), under argon, cooled to −40° C., was added triethylamine (0.41 mmol; 56 μL) then methanesulfonyl chloride (0.39 mmol; 30 μL). The reaction mixture was allowed to stir for 6 hr, with gradual warming to room temperature. The reaction was hydrolysed with saturated NH4Cl, extracted with ethyl acetate. Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (185 mg; 47%) was obtained as a light oil, after purification on preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 296(M+H)+
To a solution of 2-[4-(3-chloropropyl)-2-methoxyphenoxy]-6-fluoropyridine (0.14 mmol) in a THF/DMF mixture (340 μL/170 μL), under argon, was added NaI (0.14 mmol; 21 mg). The mixture was stirred 30 minutes at 50° C., before addition of diisopropylethylamine (0.28 mmol, 36 mg) and 1,2,4-triazol (0.28 mmol; 19 mg). The reaction mixture was allowed to stir overnight at 50° C. After concentration, the reaction was hydrolysed with saturated NH4Cl (1 mL), extracted with AcOEt (2*1 mL). Combined organic phases were dried over Na2SO4, concentrated in vacuo. The title compound (15 mg; 33%) was obtained as a yellow oil after purification on preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 329 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-fluoro-6-{2-methoxy-4-[3-(1H-1,2,4-triazol-1-yl)propyl]phenoxy}pyridine (0.05 mmol; 15 mg), the desired compound was prepared in 41% yield (6 mg) after purification by preparative TLC (dichloromethane/methanol: 9/1).
MS (ES) m/e 315(M+H+)
1H RMN (MeOD) δ (ppm): 8.48 (s, 1H); 8.02 (s, 1H); 7.85 (q, 1H, J=8.1 Hz); 6.96 (d, 1H, J=8.1 Hz); 6.79 (d, 1H, J=1.9 Hz); 6.73-6.69 (m, 2H); 6.66 (dd, 1H, J1=7.9 Hz, J2=2.2 Hz); 4.23 (t, 2H, J=7.0 Hz); 2.59 (t, 2H, J=7.6 Hz); 2.22 (qt, 2H, J=7.6 Hz).
To 4-(2-benzyloxy-4-ethylphenoxy)-3-fluoroaniline (500 mg, 1.48 mmol) in 25 ml of ethanol was added 3-bromopropylphthalimide (440 mg, 1.64 mmol). The mixture was refluxed for 2 days. The reaction mixture was diluted with ethylacetate and washed with water, saturated brine solution, dried over anhydrous Na2SO4 and concentrated. The crude obtained was passed through a silica gel column using 15% ethylacetate in petroleum ether as eluant. The LCMS of the obtained mixture showed 53% mass of the coupled product. This was taken in 25 ml of ethanol and added 7 ml of hydrazine hydrate and refluxed overnight. Ethanol was removed in vacuo and added 20% KOH solution (20 ml) to the residue. The aqueous fraction was then extracted with dichlormethane and the combined dichloromethane fraction was dried over anhydrous Na2SO4 and concentrated. The crude product obtained was purified by column chromatography using 5% methanol in dichloromethane as eluant to obtain 110 mg (18.8% after 2 steps) of the N1-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]propan-1,3-diamine.
LC-MS m/z 395.9 (M+H)+
To a solution of N1-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]propan-1,3-diamine (90 mg, 0.23 mmol) in 5 ml of dry dichloromethane and 0.08 ml (0.57 mmol) of triethylamine, cooled to 0° C., was added mesyl chloride (26 mg, 0.23 mmol) taken in 0.5 ml of dichloromethane dropwise. The reaction was quenched after 5 minutes as the reaction was complete on TLC. The reaction mixture was diluted with water and the layers separated. The aqueous layer was extracted with dichloromethane and the combined dichloromethane fraction was washed with water, dried over anhydrous Na2SO4 and concentrated. The crude residue obtained was combined with the crude obtained from an earlier 20 mg batch and column purified over silica gel using 2% methanol in dichloromethane as eluant to get 90 mg, 68.3% of title compound.
LC-MS m/z 473.2 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for N-Methanesulfonyl-N1-[4-(2-benzyloxy-4-ethylphenoxy)-3-fluorophenyl]propan-1,3-diamine (90 mg, 0.19 mmol) and tetrahydrofurane for methanol (15 mL), the title compound (50 mg, 68%) was obtained as a brown liquid, after purification on silica gel (dichloromethane/ethyl acetate: 8/2)
1H NMR (CDCl3), δ (ppm): 6.93 (t, J=8.9 Hz, 1H), 6.87 (s, 1H), 6.66-6.57 (m, 3H), 6.49 (d, J=8.1 Hz, 1H), 4.78 (bs, 1H), 3.3-3.28 (m, 4H), 2.98 (s, 3H), 2.57 (q, J=7.5 Hz, 2H), 1.92 (m, 2H), 1.21 (t, J=7.5 Hz, 3H)
LC-MS m/z 383 (M+H)+
To a solution of N1-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]propan-1,3-diamine (60 mg, 0.15 mmol) in 10 ml of dry dichloromethane, cooled to 0° C., was added acetic anhydride (20 mg, 0.19 mmol) taken in 0.5 ml of dichloromethane dropwise. The reaction mixture was warmed to rt and stirred for 1 h until reaction was complete on TLC. The reaction mixture was diluted with water and the layers separated. The aqueous layer was extracted with dichloromethane and the combined dichloromethane fraction was dried over anhydrous Na2SO4 and concentrated. The crude residue obtained was column purified over silica gel using 2% methanol in dichloromethane as eluant to get 50 mg, 75.4% of title compound.
LC-MS m/z 438.1 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for N-acetyl-N1-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]propan-1,3-diamine (70 mg, 0.16 mmol) and tetrahydrofurane for methanol (15 mL), the title compound (50 mg, 91%) was obtained as a brown liquid, after purification on silica gel (dichloromethane/ethyl acetate: 5/5)
1H NMR (CDCl3), δ (ppm): 6.93 (t, J=8.9 Hz, 1H), 6.86 (d, J=1.6 Hz, 1H), 6.64-6.58 (m, 2H), 6.46-6.42 (m, 1H), 6.36 (d, J=8.8 Hz, 1H), 5.64 (bs, 2H), 3.42-3.37 (m, 2H), 3.15 (t, J=6.4 HZ, 2H), 2.57 (q, J=7.59 Hz, 2H), 2.06 (s, 3H), 1.80 (qt, J=6.48 Hz, 2H), 1.21 (t, J=7.58 Hz, 3H)
LC-MS m/z 347.2 (M+H)+
A solution of [4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]-carbamic acid-benzyl ester (500 mg, 1.06 mmol) in 5 ml tetrahydrofuran under nitrogen atmosphere was cooled to −78° C. To this added 2.8M n-butyl lithium (0.075 g, 1.16 mmol) dropwise and the stirring at −78° C. for 1 h. Condensed ethylene oxide (0.5 ml, 9.9 mmol) was then added dropwise to the reaction mixture and warmed slowly to rt. The reaction was stirred at rt overnight and then quenched with saturated ammonium chloride solution. The aqueous phase was extracted with dichloromethane and the combined organic phase was dried over anhydrous Na2SO4 and concentrated. The crude obtained was purified by column chromatography on silica gel using 25% ethyl acetate in petroleum ether as eluant to obtain 350 mg, 81% of the title compound as a brown oil.
LC-MS m/z 407 (M+H)+
To a solution of 3-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]oxazolidin-2-one (350 mg, 0.85 mmol) in 5 ml of methanol was added barium hydroxide (245 mg, 1.28 mmol) taken in 5 ml of water. The reaction mixture was warmed to 65° C. and stirred overnight (reaction was complete on TLC). The reaction mixture concentrated in vacuo to remove methanol, diluted with water and the aqueous layer was extracted with ethyl acetate. The combined organic fraction was washed with brine, dried over anhydrous Na2SO4 and concentrated to get 300 mg, 91.57% of the title compound as a brown oil, used as such in the next step.
LC-MS m/z 382.3 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for N-[4-(2-Benzyloxy-4-ethylphenoxy)-3-fluorophenyl]-2-aminoethanol (350 mg, 0.92 mmol) and tetrahydrofurane for methanol (25 mL), the title compound (210 mg; 78%) was obtained as a yellow solid, after purification on silica gel (ethylacetate and petroleum ether: 5/5)
1H NMR (CDCl3), δ (ppm): 6.94 (t, J=8.9 Hz, 1H), 6.86 (d, J=1.2 Hz, 1H), 6.64-6.58 (m, 2H), 6.5 (dd, J=12.6 Hz, J=2.6 Hz, 1H), 6.41 (dd, J=8.7 Hz, J=2.6 Hz, 1H), 3.87 (t, J=5.1 Hz, 2H), 3.28 (t, J=5.1 Hz, 2H), 2.57 (q, J=7.58 Hz, 2H), 1.21 (t, J=7.58 Hz, 3H)
LC-MS m/z 292.3 (M+H)+
According to the procedure of example 66(a) except substituting nicotinaldehyde for propanaldehyde (28 μl, 0.45 mmol), the title compound was prepared as a colorless oil (20 mg; 18%), after purification by preparative TLC (cyclohexane/ethyl acetate: 80/20).
MS (ES) m/e 304 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 4-(4-ethyl-2-methoxyphenoxy)-3-fluoro-N-propylaniline (20 mg, 0.066 mmol), the title compound (9.4 mg, 53%) was prepared as a white solid, after purification by preparative TLC (cyclohexane/ethyl acetate: 80/20).
MS (ES) m/e 290 (M+H)+
1H NMR (CDCl3) δ (ppm): 7.28 (s, 1H), 6.93 (t, 1H, J=8.8 Hz), 6.89 (d, 1H, J=1.6 Hz), 6.70-6.56 (m, 3H), 3.10 (t, 2H, J=7.5 Hz), 2.60 (q, 2H, J=7.6 Hz); 1.72 (se, 2H, J=7.3 Hz,), 1.22 (t, 3H, J=7.6 Hz), 1.02 (t, 3H, J=7.4 Hz)
According to the procedure of example 21(a3) except substituting 4-Ethyl-2-methoxy phenol by 4-bromoguaïacol (2.51 mmol; 510 mg) and 3-Fluoro 2-nitro pyridine by 3,4-difluoronitrobenzene (2.76 mmol; 305 μL), the title compound was prepared as a clear oil in quantitative yield (855 mg) and used without further purification.
According to the procedure of example 11(a) except substituting 5-bromo-2-(2-methoxy-4-propylphenoxy)pyridine by 4-bromo-1-(2-fluoro-4-nitrophenoxy)-2-methoxybenzene (0.29 mmol; 100 mg) and 3-butyn-1-ol by 2-ethynylpyridine (0.73 mmol; 73 μL), the title compound was prepared as a yellow solid (81%; 87 mg) after purification on preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 365 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene by 2-{[4-(2-fluoro-4-nitrophenoxy)-3-methoxy phenyl]ethynyl}pyridine (0.23 mmol; 84 mg) and THF by ethanol, the title compound was obtained as a clear oil (68%, 53 mg) 10 after purification on preparative TLC (cyclohexane/ethyl acetate: 6/4).
MS (ES) m/e 339 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 3-fluoro-4-[2-methoxy-4-(2-pyridin-2-ylethyl)phenoxy]aniline (0.16 mmol; 53 mg), the title compound was prepared as a clear oil (45 mg; 15%) after purification by preparative TLC (dichloromethane/methanol/ammonia: 95/5/1).
MS (ES) m/e 325 (M+H)+
1H RMN (MeOD) δ (ppm): 8.46 (d, 1H, J=4.5 Hz); 7.78 (dt, 1H, J1=7.7 Hz, J2=1.8 Hz); 7.31-7.28 (m, 2H); 6.79 (t, 1H, J=8.9 Hz); 6.71 (s, 1H); 6.56 (dd, 1H, J1=12.7 Hz, J2=2.6 Hz); 6.51 (s, 2H); 6.47 (ddd, 1H, J1=8.7 Hz, J2=2.6 Hz, J3=1.2 Hz); 3.08-3.04 (m, 2H); 2.93-2.87 (m, 2H)
According to the procedure of example 21(a3) except substituting 4-ethyl-2-methoxyphenol by 4-bromo-5-fluoro-2-methoxyphenol (1.5 g, 5.7 mmol), the title compound was prepared in 95% yield (1.85 g) after purification on silica gel (eluant ethyl acetate/pet ether: 1/9) as a pale yellow solid.
1H NMR (CDCl3), δ (ppm): 8.25 (dd, J=4.48 Hz, J=1.28 Hz, 1H), 7.48 (dd, J=8.4 Hz, J=4.48 Hz, 1H), 7.28 (m, 1H), 7.18 (d, J=6.28 Hz, 1H), 7.01 (d, J=8.04 Hz, 1H), 3.76 (s, 3H),
LC-MS m/z 343.5 (M+H)+
According to the procedure of example 57(b) except substituting 2-(4-bromo-5-fluoro-2-methoxyphenoxy)-6-fluoropyridine by 3-(4-bromo-5-fluoro-2-methoxyphenoxy)-2-nitropyridine (1.7 g, 4.9 mmol), the title compound was obtained (1.1 g; 76%) after purification on silica gel (eluant ethyl acetate/hexane: 15/85) as a pale yellow solid.
1H NMR (CDCl3), δ (ppm): 8.23 (dd, J=4.4 Hz, J=0.8 Hz, 1H), 7.47 (dd, J=8.4 Hz, J=4.8 Hz, 1H), 7.3 (dd, J=8.4 Hz, J=0.8 Hz, 1H), 7.08 (d, J=6.8 Hz, 1H), 6.91 (d, J=10 Hz, 1H), 6.85 (dd, J=17.6 Hz, J=11.2 Hz, 1H), 5.81 (d, J=17.6 Hz, 2H), 5.43 (d, J=11.2 Hz, 3H), 3.78 (s, 3H),
LC-MS m/z 290.9 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene by 3-(5-fluoro-2-methoxy-4-vinylphenoxy)-2-nitropyridine (3.7 mmol, 1.1 g) and THF by methanol, the title compound was prepared as a white solid (800 mg; 80.5%) and used without further purification.
1H NMR (CDCl3), δ (ppm): 7.82 (dd, J=4.8 Hz, J=1.2 Hz, 1H), 6.89 (dd, J=8 Hz, J=1.2 Hz, 1H), 6.8 (d, J=6.8 Hz, 1H), 6.67 (d, J=10 Hz, 1H), 6.57-6.6.6 (m, 1H), 4.76 (bs, 2H, D2O exchangeable), 3.82 (s, 3H), 2.66 (q, J=7.6 Hz, 2H), 1.24 (t, J=7.6 Hz, 3H)
LC-MS m/z 263 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 3-(4-Ethyl-5-fluoro-2-methoxy-phenoxy)-2-aminopyridine (400 mg, 1.53 mmol), the title compound was prepared in 86% yield (325 mg) as a white solid after washing with hexane.
1H NMR (CDCl3), δ (ppm): 7.85 (dd, J=5.2 Hz, J=1.2 Hz, 1H), 6.98 (d, J=8 Hz, J=1.2Hz, 1H), 6.89 (d, J=7.6 Hz, 1H), 6.58-6.64 (m, 2H), 4.67 (bs, 2H, D2O exchangeable), 2.62 (q, J=7.6 Hz, 2H), 1.23 (t, J=7.6 Hz, 3H)
LC-MS m/z 249.1 (M+H)+
To a solution of 1-[4-(4-ethyl-2-hydroxyphenoxy)-3-fluorophenyl]ethanone (0.37 mmol; 100 mg) in dry THF (2 mL) cooled to 0° C. were added, N-Boc-glycine (0.37 mmol; 64 mg), benzotriazol-1-yloxytris(dimethylamino)phosphoniumhexafluoro phosphate (0.37 mmol; 190 mg) and triethylamine (1.09 mmol; 153 μL). The reaction was stirred at 0° C. for 3 hours and overnight at room temperature. The mixture was concentrated, treated with saturated NH4Cl and extracted with dichloromethane. Combined organic phases were washed with water, dried over Na2SO4 and concentrated in vacuo. The title compound (91 mg; 58%) was obtained as clear oil after purification on preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 454 (M+Na)+
To a solution of tert-Butoxycarbonylamino-acetic acid 2-(4-acetyl-2-fluoro-phenoxy)-5-ethyl-phenyl ester (0.21 mmol; 91 mg) in dry dioxane (1 mL) cooled to 0° C., was added HCl/dioxane 4M (0.84 mmol; 211 μL). The reaction was stirred overnight at room temperature. A precipitate was formed. The mixture was cooled to 0° C., filtered and the solid was washed with diethylether. This white solid was dried in vacuo to give the title compound (8%; 7 mg).
1H RMN (MeOD) δ (ppm): 7.85 (dd, 1H, J1=11.5 Hz, J2=2.0 Hz); 7.78 (d, 1H, J=8.7 Hz); 7.23-7.20 (m, 2H); 7.06-7.02 (m, 2H); 4.06 (s, 2H); 2.70 (q, 2H, J=7.6 Hz); 2.57 (s, 3H); 1.27 (t, 3H, J=7.6 Hz).
To a solution of N,O-dimethylhydroxylamine (1.51 mmol; 147 mg) in dry THF (3 mL), under argon, was added at −78° C. nbutyllithium 2.5M (3.02 mmol; 1.21 mL). The mixture was stirred 30 minutes at −78° C., before addition of 4-fluorobenzoyl chloride (1.26 mmol; 150 μL). The reaction was stirred overnight at room temperature, then treated with saturated NH4Cl and extracted with ethyl acetate. Combined organic layers were washed with water, dried over Na2SO4 and concentrated in vacuo, to give the title compound (66%; 173 mg) as a yellow oil used without further purification.
1H RMN (CDCl3) δ (ppm): 7.78 (m, 2H); 7.10 (t, 2H, J=8.7 Hz); 3.56 (s, 3H); 3.38 (s, 3H).
To a solution of 4-fluoro-N-methoxy-N-methylbenzamide (0.94 mmol; 173 mg) in anhydrous THF (2 mL), at −78° C. under argon, was added a solution of (1,3-dioxan-2-ylethyl)magnesium bromide, 0.5M in THF (1.04 mmol; 2.1 mL). The reaction was stirred 16 hours at room temperature. The mixture was cooled to −78° C. and (1,3-dioxan-2-ylethyl)magnesium bromide, 0.5M in THF (2.00 mmol; 4 mL) was added again. The reaction was stirred overnight at room temperature. The mixture was treated with saturated NH4Cl and extracted with ethyl acetate. The organic layer was washed with water, dried over Na2SO4, and concentrated in vacuo. The title compound was prepared in quantitative yield, used without further purification.
MS (ES) m/e 239 (M+H)+
According to the procedure of example 21(a3) except substituting 3-Fluoro 2-nitro pyridine by 3-(1,3-dioxan-2-yl)-1-(4-fluorophenyl)propan-1-one (0.94 mmol; 401 mg), the title compound was obtained (42%, 149 mg) as a yellow oil after purification on preparative TLC (cyclohexane/ethyl acetate: 8/2).
MS (ES) m/e 371 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 1-[4-(4-ethyl-2-methoxyphenoxy)phenyl]-3-(1,3-dioxan-2-yl)-1-phenylpropan-1-one (0.25 mmol; 91 mg), the following compounds were obtained after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3):
3-(1,3-dioxan-2-yl)-1-[4-(4-ethyl-2-hydroxyphenoxy)phenyl]propan-1-one (11 mg; 13%) as a white solid
MS (ES) m/e 357 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.95 (d, 2H, J=8.9 Hz); 7.00 (d, 2H, J=8.9 Hz); 6.91 (d, 1H, J=1.9 Hz); 6.87 (d, 1H, J=8.2 Hz); 6.73 (dd, 1H, J1=8.2 Hz, J2=1.9 Hz); 5.46 (sl, 1H); 4.66 (t, 1H, J=4.9 Hz); 4.09 (dd, 2H, J1=10.7 Hz, J2=4.9 Hz); 3.76 (td, 2H, J1=12.1 Hz, J2=2.4 Hz);
3.05 (t, 2H, J=7.2 Hz); 2.63 (q, 2H, J=7.6 Hz); 2.06-2.01 (m, 3H); 1.33 (d, 1H, J=13.4 Hz); 1.22 (t, 3H, J=7.6 Hz).
4-[4-(4-ethyl-2-hydroxyphenoxy)phenyl]-4-oxobutanal (12.5 mg; 17%) as a clear oil.
MS (ES) m/e 299(M+H+)
To a suspension of NaBH4 (0.052 mmol; 2 mg) in dry methanol, under argon at −78° C., (0.5 mL) was added 4-[4-(4-ethyl-2-hydroxyphenoxy)phenyl]-4-oxobutanal (0.040 mmol; 12 mg). The reaction was stirred 5 hours with gradual warming to −5° C., and treated with acetic acid. The mixture was diluted with water and extracted with ethyl acetate. Combined organic layers were dried over Na2SO4 and concentrated in vacuo. The title compound was obtained as a clear oil (7.6 mg; 63%) after purification on preparative TLC (cyclohexane/ethyl acetate: 5/5).
MS (ES) m/e 301(M+H+)
1H RMN (CDCl3) δ (ppm): 7.30 (d, 2H, J=8.5 Hz); 6.97 (d, 2H, J=8.6 Hz); 6.89 (d, 1H, 1.9 Hz); 6.80 (d, 1H, J=8.2 Hz); 6.68 (dd, 1H, J1=8.1 Hz, J2=2.0 Hz); 4.70 (t, 1H, J=6.3 Hz); 3.69 (se, 2H, J=5.8 Hz); 2.61 (q, 2H, J=7.6 Hz); 1.85 (q, 2H, J=6.6 Hz); 1.68 (se, 2H, J=7.0 Hz); 1.23 (t, 3H, J=7.6 Hz).
To a stirred solution of 2-(2-aminopyridin-3yloxy)-5-ethyl-4-fluorophenol (45 mg, 0.18 mmol) in glacial acetic acid (2.5 ml) was added 0.36 ml of tetrafluoroboric acid (48% in water). The reaction mixture was cooled to 0° C. and sodium nitrite (18 mg, 0.27 mmol) was added at 0° C. and stirred at 0° C. for 1.5 hours until reaction was complete on TLC. The reaction mixture was quenched by adding ice and sodium bicarbonate solution and stirred for 10 minutes before extracting the aqueous solution with ethylacetate. The combined ethyl acetate fraction was washed with saturated sodium bicarbonate solution, water, followed by brine, dried over anhydrous sodium sulfate and concentrated in vacuo to get the crude compound. The crude material was column purified over silica gel using Petroleum ether/ethyl acetate 9:1 as eluant and then further purified by preparative HPLC using 0.1% TFA in water and acetonitrile as solvent system to get 8 mg (17.6%) of 5-Ethyl-4-fluoro-2-(2-fluoropyridin-3yloxy)phenol as a white solid.
1H NMR (CDCl3), δ (ppm): 8.01-8.98 (m, 1H), 7.43-7.39 (m, 1H), 7.17-7.20 (m, 1H), 6.91 (d, J=7.2 Hz, 1H), 6.57 (d, J=9.6 Hz, 1H), 5.35 (s, 1H, D2O exchangeable), 2.63 (q, J=7.5 Hz, 2H), 1.25 (t, J=7.5 Hz, 3H)
LC-MS m/z 252 (M+H)
Alternatively the title compound can be synthesized from 3-(4-Ethyl-5-fluoro-2-methoxy-phenoxy)-2-aminopyridine of step c) of example 84 according to following steps:
To a stirred solution of 3-(4-Ethyl-5-fluoro-2-methoxy-phenoxy)-2-aminopyridine (1.5 g, 5.7 mmol) in glacial acetic acid (10 ml) was added 12 ml of tetrafluoroboric acid (48% in water). The reaction mixture was cooled to 0° C. and sodium nitrite (590 mg, 8.5 mmol) was added at 0° C. and stirred at 0° C. for 45 minutes until reaction was complete on TLC. Formation of 2 compounds was observed on the TLC. The colourless reaction mixture turned pale yellow and then to deep yellow during this time. The reaction mixture was quenched by adding ice and sodium bicarbonate solution and the aqueous solution was extracted with ethyl acetate. The combined ethyl acetate fraction was washed with water, followed by brine, dried over anhydrous sodium sulfate and concentrated in vacuo to get the crude compound. The crude material was column purified over silica gel using pet ether/ethyl acetate 9:1 as eluant to obtain the first fraction yielding 610 mg, 40.39% of the title compound 3-(4-Ethyl-5-fluoro-2-methoxy-phenoxy)-2-fluoro pyridine as a colourless liquid. The column was then eluted with 100% ethyl acetate to collect the second fraction that gave 620 mg, 41.3% of the 3-(4-Ethyl-5-fluoro-2-methoxy-phenoxy)-pyridin-2-ol.
1H NMR (CDCl3), δ (ppm): 7.90-7.89 (m, 1H), 7.20 (t, J=8 Hz, 1H), 7.1-7.07 (m, 1H), 6.82 (d, J=6.96 Hz, 1H), 6.73 (d, J=9.68 Hz, 1H), 3.8 (s, 3H), 2.67 (q, J=7.53 Hz, 2H), 1.25 (t, J=7.58 Hz, 3H)
LC-MS m/z 266.2 (M+H)+
1H NMR (CDCl3), δ (ppm): 7.15 (d, J=6.44 Hz, 1H), 6.82-6.78 (m, 2H), 6.72 (d, J=7.2 Hz, 1H), 6.17 (t, J=7.2 Hz, 1H), 3.81 (s, 3H), 2.67 (q, J=7.5 Hz, 2H), 1.27 (t, J=7.5 Hz, 3H)
LC-MS m/z 264.1 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine by 3-(4-Ethyl-5-fluoro-2-methoxy-phenoxy)-2-fluoro pyridine (610 mg, 2.3 mmol), the title compound was prepared in 81% yield (470 mg) as a white solid after washing with hexane.
According to the procedure of example 70(a) except substituting N-Acetylethylenediamine for ethylamine.HCl ((8.4 mmol; 700 mg), the title compound (402 mg; 0.94 mmol; 25%) was obtained as a yellow oil, after purification on silica gel (gradient cyclohexane/dichloromethane/ethyl acetate).
MS (ES) m/e 430 (M+H)+
According to the procedure of example 20(b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl)phenoxy]benzene for 4-(2-Benzyloxy-4-ethyl-phenoxy)-N-ethyl-3-fluoro-benzene sulfonamide (402 mg; 0.94 mmol) and tetrahydrofurane for ethanol (4 mL), the title compound (140 mg; 44%) was obtained as a clear oil, after purification on preparative TLC (dichloromethane).
MS (ES) m/e 340 (M+H)+
1H RMN (CDCl3) δ (ppm): 7.63 (d, 1H, J=10.0 Hz); 7.53 (d, 1H, J=8.7 Hz); 6.95 (d, 1H, J=8.2 Hz); 6.92 (s, 1H); 6.87 (d, 1H, J=8.2 Hz); 6.74 (d, 1H, J=8.2 Hz); 6.03 (br, 1H); 5.01 (t, 1H, J=5.9 Hz); 3.00 (qt, 2H, J=7.0 Hz); 2.62 (q, 2H, J=7.6 Hz); 1.23 (t, 3H, J=7.6 Hz); 1.10 (t, 3H, J=7.3 Hz).
To a solution of 3-fluoropyridine (2.3 mmol; 220 mg), under argon, in anhydrous THF (1 mL) cooled to −78° C., was added nBuLi (2.3 mmol; 1 mL). The reaction was stirred 1 hr at −78° C. then a solution of vanilline-OTBS (2.3 mmol; 600 mg) in THF (1 mL) was added. The reaction was allowed to warm up to room temperature overnight. Hydrolysed by NH4Cl sat. (3 mL), the mixture was extracted with dichloromethane (3 mL) and ethyl acetate (2*3 mL). Combined organic phases were dried over MgSO4, concentrated to yield a light brown solid. Heating in diethyl ether, then filtering afforded the title compound as a white solid (125 mg; 0.34 mmol; 15%) used without further purification.
MS (ES) m/e 364 (M+H)+
Pd/C (0.02 mmol; 40 mg) was added to a solution of [4-(tert-Butyl-dimethyl-silanyloxy)-3-methoxy-phenyl]-(3-fluoro-pyridin-4-yl)-methanol (0.19 mmol; 70 mg) in methanol (2 mL) and H2SO4 (0.5 mL). The mixture was flushed twice with hydrogen, and the reaction was stirred overnight at 35° C. The mixture was filtered on celite, washed with methanol. After concentration, water was added (3 mL) and K2CO3 until pH 8. The aqueous phase was extracted with ethyl acetate (2*3 mL). Combined organic phases were dried over MgSO4, concentrated to yield the title compound as a white solid (32 mg; 0.14 mmol; 71%) used as such.
MS (ES) m/e 234 (M+H)+
According to the procedure of example 21(a3) except substituting 4-Ethyl-2-methoxy phenol for 4-[(3-fluoropyridin-4-yl)methyl]-2-methoxyphenol (60 mg; 0.26 mmol), the title compound (85 mg; 100%) was prepared as a brown oil, used without any purification.
MS (ES) m/e 329 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-fluoro-6-{4-[(3-fluoropyridin-4-yl)methyl]-2-methoxyphenoxy}pyridine (85 mg; 0.26 mmol), the title compound (23 mg; 28%) was prepared as a clear oil, after purification by preparative TLC (dichloromethane/ethyl acetate).
MS (ES) m/e 315 (M+H)+
1H RMN (CDCl3) δ (ppm): 8.37 (s, 1H); 8.27 (d, 1H, J=4.7 Hz); 7.76 (q, 1H, J=8.0 Hz); 7.12 (t, 1H, J=5.7 Hz); 7.06 (d, 1H, J=8.2 Hz); 6.83 (d, 1H, J=1.8 Hz); 6.79-6.75 (m, 2H); 6.62 (dd, 1H, J1=7.9 Hz, J2=2.1 Hz); 3.98 (s, 2H).
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 3-(4-Ethyl-5-fluoro-2-methoxy-phenoxy)-pyridin-2-ol (50 mg, 0.19 mmol), the title compound (25 mg; 53%) was prepared as a white solid, after washing with hexane twice and with diethylether MS (ES) m/e 315 (M+H)+
1H NMR (CD3OD), δ (ppm): 7.18 (d, J=6.5 Hz, 1H), 6.96 (d, J=7.4 Hz, 1H), 6.81 (d, J=7.4 Hz, 1H), 6.74 (d, J=10.1 Hz, 1H), 6.32 (t, J=6.98 Hz, 1H), 2.6 (q, J=7.5 Hz, 2H), 1.2 (t, J=7.5 Hz, 3H)
LC-MS m/z 250 (M+H)+
According to the procedure of example 42(a) except substituting 3-chloropropanesulfonyle chloride by 2-phtalimido ethanesulfonyl chloride (0.46 mmol; 125 mg), the title compound (77%; 147 mg) was obtained as a white gum after purification on preparative TLC (cyclohexane/ethyl acetate: 6/4).
MS (ES) m/e 499 (M+H)+
According to the procedure of example 1(b) except substituting 6-chloro-2-(2-methoxy-4-propylphenoxy)pyridin-3-amine for 2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-ethane sulfonic acid [4-(4-ethyl-2-methoxy-phenoxy)-3-fluoro-phenyl]-amide (0.30 mmol; 147 mg), the desired compound was prepared in 55% yield (79 mg) after purification by preparative TLC (cyclohexane/ethyl acetate: 7/3).
MS (ES) m/e 485(M+H+)
1H RMN (CDCl3) δ (ppm): 7.86 (dd, 2H, J1=5.5 Hz, J2=3.1 Hz); 7.75 (dd, 2H, J1=5.4 Hz, J2=3.0 Hz); 7.4 3 (s, 1H); 7.23 (dd, 1H, J1=11.5 Hz, J2=2.4 Hz); 7.01 (d, 1H, J=8.8 Hz); 6.93 (t, 1H, J=8.6 Hz); 6.88 (d, 1H, J=1.77 Hz); 6.71 (d, 1H, J=8.2 Hz); 6.65 (dd, 1H, J1=8.3 Hz, J2=1.9 Hz); 5.82 (sl, 1H); 4.15 (t, 2H, J=6.3 Hz); 3.48 (t, 2H, J=6.2 Hz); 2.59 (q, 2H, J=7.6 Hz); 1.22 (t, 3H, J=7.6 Hz).
According to the procedure of example 39 except substituting 2-{3-[4-(4-Ethyl-2-hydroxy-phenoxy)-3-fluoro-phenoxy]-propyl}-isoindole-1,3-dione by 2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-ethanesulfonic acid [4-(4-ethyl-2-hydroxy-phenoxy)-3-fluoro-phenyl]-amide (0.13 mmol; 64 mg), the title compound was obtained as a yellow oil (20%, 10 mg) after purification on preparative TLC (dichloromethane/methanol/ammonia: 90/10/1).
MS (ES) m/e 355 (M+H)+
1H RMN (MeOD) δ (ppm): 7.22 (dd, 1H, J1=12.3 Hz, J2=2.5 Hz); 6.99 (d, 1H, J=8.8 Hz); 6.84-6.79 (m, 2H); 6.74 (d, 1H, J=8.2 Hz); 6.64 (dd, 1H, J1=8.2 Hz, J2=1.9 Hz); 3.25 (t, 2H, J=6.7 Hz); 3.10 (t, 2H, J=6.5 Hz); 2.57 (q, 2H, J=7.6 Hz); 1.21 (t, 3H, J=7.6 Hz).
The compounds of the present invention are useful inhibitors of bacterial FabI enzyme.
Compound inhibitory activity of FabI enzyme is measured in vitro by the IC50 determination using a fluorescent based assay.
The protein FabI from E. coli is prepared and purified using standard methods for recombinant protein expression after cloning of the gene in a prokaryotic expression vector.
The biochemical activity of the FabI enzyme is assessed using the following method.
The assay buffer “AB” contains 50 mM Hepes pH7.5, 100 μM Dithiothreitol, 0.006% Triton-X100. The following components are added in a black polystyrene Costar plate up to a final volume of 55 μL: 1.5 μL DMSO, or inhibitor dissolved in DMSO and 53.5 μL of a FabI/NADH/NAD+ mixture in AB. After 60 min of pre-incubation at room temperature, the reaction is started by addition of 5 μL of Crotonoyl-CoA to a final volume of 60 μL. This reaction mixture is then composed of 40 nM FabI (produced in house from E. coli, C-terminal 6-His tagged), 20 μM NADH (Biochemika), 10 μM NAD+ (Biochemika), 50 μM Crotonoyl-CoA (Biochemika) and compound at defined concentration. Fluorescence intensity of NADH (lex=360 nm, lem=520 nm) is measured immediately after Crotonoyl-CoA addition, and 2 hours later by a Fluostar Optima (BMG). Enzyme activity is proportional to the signal decrease from which inhibition percentages are derived. For IC50 determinations, the inhibitor is tested at 6 to 10 different concentrations, and the related inhibitions are fitted to a classical langmuir equilibrium model using XLFIT (IDBS).
In vitro Inhibition of Recombinant E. coli FabI Enzyme by Selected Compounds of Formula (I).
The compounds of the present invention are useful antibacterial agents having a selective spectrum of activity in vitro against standard bacterial strains which are used to screen for activity against pathogenic bacteria. Notably the compounds of the present invention show activity against Staphyloccus aureus including multiresistant strains and Escherichia coli. The activity is presented as Minimum Inhibitory Concentration (MIC) expressed in μg/ml.
Whole-cell antimicrobial activity was determined by broth microdilution method in microtiterplates. The compound was tested in serial 4-fold dilutions ranging from 0.06 to 64 mcg/mL. Test organisms were selected from the following laboratory strains: Staphylococcus aureus CIP 76.25, Staphylococcus aureus BAA39 MDR, Staphylococcus aureus NEM 14157 PeniR, Staphylococcus aureus CIP 54.146, Escherichia coli CIP 76.24. Bacteria were tested in Tryptic Soy (TS) or Mueller Hinton (MH) broth using an inoculum of 104 to 106 UFC/mL incubated at 37° C. for 20 h.
The minimum inhibitory concentration (MIC) was determined as the lowest concentration of compound at which no visible bacteria growth is observed (90% inhibition of absorbance of at 600 nM.)
E. coli
S. aureus
S. aureus
S. aureus
S. aureus
S. aureus
S. aureus
S. aureus
S. aureus
S. aureus
In vivo Antibacterial Activity of Compounds
An experimental model of infection by S. aureus was used to assess the antibacterial activity of FabI inhibitors.
Briefly in vivo studies were performed using 5-6-week-old female BALB/c@Rj mice as follows Groups of six mice are used for each condition.
The virulent strain of Staphylococcus aureus CIP 54.146 is grown to exponential phase in Tryptic soy (TS) broth culture. The bacterial culture is diluted to obtain a bacterial suspension of 1.108 UFC/ml. Then 200 μl of the suspension is administered by intraperitoneal injection to each mouse, this infecting dose has been determined to be the LD90 (Lethal dose 90%). The inoculums count was determined by plating 10-fold dilutions of the suspension on TH agar plates immediately after inoculation.
Compounds to be assessed are dissolved and diluted in an aqueous solution containing 15% cyclodextrin and 200 μl of the solution is injected sub cuteanously to each mice, just after the infection.
For 48 hours post-infection, mice are monitored and survival recorded at 18 h and 24 h postinfection. The negative control group receives the 15% cyclodextrin solution alone and vancomycin at 10 mg/kg is used as the positive control.
All animal experiments were carried out in accordance with institutional guidelines. Compound activity is measure by its effect at a given dose on the percentage of surviving animal.
As shown in
An injectable preparation was prepared comprising 500 mg of a compound of example 87 and sufficient quantity of aqueous sterile excipient for preparing 10 to 50 ml of injectable solution.
Tablets have been prepared containing:
| Number | Date | Country | Kind |
|---|---|---|---|
| 06290611.0 | Apr 2006 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB2007/002127 | 4/16/2007 | WO | 00 | 10/14/2008 |
